[
  {
    "phenotype_id": "PH2700",
    "phenotype_version_id": 6739,
    "name": "Immunosuppression codes (persisting)",
    "definition": "This codelist was taken from [OpenCodelists](https://www.opencodelists.org/), created by [OpenSAFELY](https://www.opensafely.org/). We recommend viewing this Phenotype on the OpenCodelist website to view the most recent version.\n\n\nTaken from the `IMATRISK1_COD` refset published by NHSD. Contains public sector information licensed under the UK Open Government Licence v3\\.0 (https://www.nationalarchives.gov.uk/doc/open\\-government\\-licence/version/3/).\n\n\n© University of Oxford for the Bennett Institute for Applied Data Science 2025\\. This work may be copied freely for non\\-commercial research and study.\n\n",
    "implementation": null,
    "publications": null,
    "validation": null,
    "citation_requirements": null,
    "created": "2026-01-26T22:37:33.335701Z",
    "author": "NHSD Primary Care Domain Refsets",
    "collections": [
      {
        "name": "OpenCodelist",
        "value": 31
      },
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": {
      "id": 1,
      "slug": "opensafely",
      "name": "OpenSAFELY"
    },
    "world_access": 1,
    "updated": "2026-01-26T22:38:06.395641Z",
    "references": [
      {
        "url": "https://digital.nhs.uk/data-and-information/data-collections-and-data-sets/data-collections/quality-and-outcomes-framework-qof/quality-and-outcome-framework-qof-business-rules/primary-care-domain-reference-set-portal",
        "title": "Primary Care Domain Reference Set Portal"
      }
    ],
    "signed_off": [],
    "methodology": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "nhsd-primary-care-domain-refsets/imatrisk1_cod",
    "source_reference": "https://www.opencodelists.org/codelist/nhsd-primary-care-domain-refsets/imatrisk1_cod/20250912",
    "concept_information": [
      {
        "concept_id": 6916,
        "concept_version_id": 14401,
        "concept_name": "nhsd-primary-care-domain-refsets/imatrisk1_cod/20250912",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH2700",
        "phenotype_version_id": 6739,
        "phenotype_name": "Immunosuppression codes (persisting)",
        "code_attribute_header": [],
        "codes": [
          {
            "code": "1003381002",
            "description": "Onycho-tricho-dysplasia neutropenia syndrome",
            "attributes": null
          },
          {
            "code": "1003551006",
            "description": "Agenesis of spleen",
            "attributes": null
          },
          {
            "code": "10294000",
            "description": "Reactive mastocytosis",
            "attributes": null
          },
          {
            "code": "1052325005",
            "description": "Exacerbation of psoriasis due to human immunodeficiency virus infection",
            "attributes": null
          },
          {
            "code": "105601003",
            "description": "Quantitative disorder of neutrophils",
            "attributes": null
          },
          {
            "code": "105602005",
            "description": "Quantitative abnormality of granulocytes",
            "attributes": null
          },
          {
            "code": "10564005",
            "description": "Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin",
            "attributes": null
          },
          {
            "code": "10755671000119100",
            "description": "Human immunodeficiency virus in mother complicating childbirth",
            "attributes": null
          },
          {
            "code": "10759351000119103",
            "description": "Sickle cell anemia in mother complicating childbirth",
            "attributes": null
          },
          {
            "code": "108521000119103",
            "description": "History of reticulosarcoma",
            "attributes": null
          },
          {
            "code": "108631000119101",
            "description": "History of autologous bone marrow transplant",
            "attributes": null
          },
          {
            "code": "1090241000000107",
            "description": "Angioimmunoblastic T-cell lymphoma with dysproteinaemia",
            "attributes": null
          },
          {
            "code": "1091861000000100",
            "description": "Follicular lymphoma, cutaneous follicle centre",
            "attributes": null
          },
          {
            "code": "1091891000000106",
            "description": "B-cell Hodgkin's lymphoma",
            "attributes": null
          },
          {
            "code": "1091921000000103",
            "description": "B-cell non-Hodgkin's lymphoma",
            "attributes": null
          },
          {
            "code": "109962001",
            "description": "Diffuse non-Hodgkin's lymphoma",
            "attributes": null
          },
          {
            "code": "109964000",
            "description": "Diffuse non-Hodgkin's lymphoma, undifferentiated",
            "attributes": null
          },
          {
            "code": "109965004",
            "description": "Diffuse non-Hodgkin's lymphoma, lymphoblastic",
            "attributes": null
          },
          {
            "code": "109966003",
            "description": "Diffuse non-Hodgkin's lymphoma, immunoblastic",
            "attributes": null
          },
          {
            "code": "109967007",
            "description": "Diffuse non-Hodgkin's lymphoma, small cleaved cell",
            "attributes": null
          },
          {
            "code": "109968002",
            "description": "Diffuse non-Hodgkin's lymphoma, small cell",
            "attributes": null
          },
          {
            "code": "109969005",
            "description": "Diffuse large B-cell malignant lymphoma",
            "attributes": null
          },
          {
            "code": "109970006",
            "description": "Follicular non-Hodgkin's lymphoma, small cleaved cell",
            "attributes": null
          },
          {
            "code": "109971005",
            "description": "Follicular non-Hodgkin's lymphoma, mixed small cleaved cell and large cell",
            "attributes": null
          },
          {
            "code": "109972003",
            "description": "Follicular non-Hodgkin's lymphoma, large cell",
            "attributes": null
          },
          {
            "code": "109975001",
            "description": "T-zone lymphoma",
            "attributes": null
          },
          {
            "code": "109976000",
            "description": "Lymphoepithelioid lymphoma",
            "attributes": null
          },
          {
            "code": "109977009",
            "description": "Peripheral T-cell lymphoma",
            "attributes": null
          },
          {
            "code": "109978004",
            "description": "T-cell lymphoma",
            "attributes": null
          },
          {
            "code": "109979007",
            "description": "B-cell lymphoma",
            "attributes": null
          },
          {
            "code": "109981009",
            "description": "Waldenström macroglobulinemia",
            "attributes": null
          },
          {
            "code": "109982002",
            "description": "Alpha heavy chain disease",
            "attributes": null
          },
          {
            "code": "109983007",
            "description": "Monoclonal gammopathy",
            "attributes": null
          },
          {
            "code": "109984001",
            "description": "Gamma heavy chain disease",
            "attributes": null
          },
          {
            "code": "109985000",
            "description": "Immunoproliferative small intestinal disease",
            "attributes": null
          },
          {
            "code": "109989006",
            "description": "Multiple myeloma",
            "attributes": null
          },
          {
            "code": "109991003",
            "description": "Acute panmyelosis with myelofibrosis",
            "attributes": null
          },
          {
            "code": "109993000",
            "description": "Chronic myeloproliferative disorder (clinical)",
            "attributes": null
          },
          {
            "code": "109996008",
            "description": "Myelodysplastic syndrome: Refractory anemia, without ringed sideroblasts, without excess blasts",
            "attributes": null
          },
          {
            "code": "110000005",
            "description": "Refractory anemia with excess blasts in transformation",
            "attributes": null
          },
          {
            "code": "110002002",
            "description": "Mast cell leukemia",
            "attributes": null
          },
          {
            "code": "110004001",
            "description": "Acute promyelocytic leukemia, FAB M3",
            "attributes": null
          },
          {
            "code": "110005000",
            "description": "Acute myelomonocytic leukemia, FAB M4",
            "attributes": null
          },
          {
            "code": "110006004",
            "description": "Prolymphocytic leukemia",
            "attributes": null
          },
          {
            "code": "110007008",
            "description": "Adult T-cell leukemia/lymphoma",
            "attributes": null
          },
          {
            "code": "111037009",
            "description": "Basophilic hyperplasia",
            "attributes": null
          },
          {
            "code": "111396008",
            "description": "Chédiak-Higashi syndrome",
            "attributes": null
          },
          {
            "code": "111583006",
            "description": "Leukocytosis",
            "attributes": null
          },
          {
            "code": "111584000",
            "description": "Reticular dysgenesis",
            "attributes": null
          },
          {
            "code": "111585004",
            "description": "Neutropenia associated with autoimmune disease",
            "attributes": null
          },
          {
            "code": "111587007",
            "description": "Severe combined immunodeficiency due to absent interleukin-2 receptor",
            "attributes": null
          },
          {
            "code": "111880001",
            "description": "Acute human immunodeficiency virus infection",
            "attributes": null
          },
          {
            "code": "1142045004",
            "description": "Primary human immunodeficiency virus infection",
            "attributes": null
          },
          {
            "code": "1142046003",
            "description": "Pityriasis rubra pilaris due to human immunodeficiency virus infection",
            "attributes": null
          },
          {
            "code": "1142049005",
            "description": "Parasitic disease due to human immunodeficiency virus infection",
            "attributes": null
          },
          {
            "code": "1142055000",
            "description": "Human immunodeficiency virus modified skin disease",
            "attributes": null
          },
          {
            "code": "1144907001",
            "description": "Late acute graft-versus-host disease",
            "attributes": null
          },
          {
            "code": "1144908006",
            "description": "Late chronic graft-versus-host disease",
            "attributes": null
          },
          {
            "code": "1144933009",
            "description": "Recurrent infection due to immunoglobulin isotype deficiency",
            "attributes": null
          },
          {
            "code": "1144963000",
            "description": "Acute on chronic graft-versus-host disease",
            "attributes": null
          },
          {
            "code": "1148845007",
            "description": "Follicular lymphoma grade 3b",
            "attributes": null
          },
          {
            "code": "1148851002",
            "description": "Follicular lymphoma grade 3a",
            "attributes": null
          },
          {
            "code": "1148863007",
            "description": "Disorder of skin due to human immunodeficiency virus infection",
            "attributes": null
          },
          {
            "code": "1148888004",
            "description": "Nodular glomerulosclerosis due to heavy chain deposition disease",
            "attributes": null
          },
          {
            "code": "1148890003",
            "description": "Hemophagocytic lymphohistiocytosis due to malignant disease",
            "attributes": null
          },
          {
            "code": "1148906001",
            "description": "Acute myeloid leukemia with t(8;21)(q22;q22) RUNX1-RUNX1T1",
            "attributes": null
          },
          {
            "code": "1148911004",
            "description": "Gouty arthropathy due to double heterozygous sickling disorder",
            "attributes": null
          },
          {
            "code": "1148919002",
            "description": "Disorder of glomerulus due to double heterozygous sickling disorder",
            "attributes": null
          },
          {
            "code": "1153336009",
            "description": "Pediatric nodal marginal zone B cell lymphoma",
            "attributes": null
          },
          {
            "code": "1153341001",
            "description": "Myeloproliferative hypereosinophilic syndrome",
            "attributes": null
          },
          {
            "code": "1153346006",
            "description": "Primary non-Hodgkin malignant lymphoma of uveal tract",
            "attributes": null
          },
          {
            "code": "1153347002",
            "description": "Primary non-Hodgkin malignant lymphoma of vitreoretinal tract",
            "attributes": null
          },
          {
            "code": "1153348007",
            "description": "Primary effusion lymphoma due to human immune deficiency virus infection",
            "attributes": null
          },
          {
            "code": "1153354008",
            "description": "Malignant lymphoma of duodenum",
            "attributes": null
          },
          {
            "code": "1153355009",
            "description": "Malignant lymphoma of esophagus",
            "attributes": null
          },
          {
            "code": "1153356005",
            "description": "Lymphoma of anus",
            "attributes": null
          },
          {
            "code": "1153357001",
            "description": "Lymphoma of appendix",
            "attributes": null
          },
          {
            "code": "1153374001",
            "description": "Myelofibrosis caused by drug",
            "attributes": null
          },
          {
            "code": "1153377008",
            "description": "Mixed phenotype acute leukemia with t(9;22) (q34;q11.2); BCR-ABL1",
            "attributes": null
          },
          {
            "code": "1153379006",
            "description": "Mixed phenotype acute leukemia with T-cell and myeloid lineage",
            "attributes": null
          },
          {
            "code": "1153381008",
            "description": "Mixed phenotype acute leukemia with myeloid and B-cell lymphoid phenotypes",
            "attributes": null
          },
          {
            "code": "1153382001",
            "description": "Malignant lymphoma of lacrimal gland",
            "attributes": null
          },
          {
            "code": "1153383006",
            "description": "Malignant lymphoma of liver",
            "attributes": null
          },
          {
            "code": "1153397003",
            "description": "Hydroa vacciniforme-like cutaneous T-cell lymphoma",
            "attributes": null
          },
          {
            "code": "1153412006",
            "description": "Acute chest syndrome due to sickle cell thalassemia with crisis",
            "attributes": null
          },
          {
            "code": "1153413001",
            "description": "Acute sequestration of spleen due to sickle cell thalassemia with crisis",
            "attributes": null
          },
          {
            "code": "1153414007",
            "description": "Acute chest syndrome due to sickle cell hemoglobin C disease with crisis",
            "attributes": null
          },
          {
            "code": "1153415008",
            "description": "Acute sequestration of spleen due to sickle cell hemoglobin C disease with crisis",
            "attributes": null
          },
          {
            "code": "1153417000",
            "description": "Secondary hemophagocytic lymphohistiocytosis",
            "attributes": null
          },
          {
            "code": "1156296001",
            "description": "Acquired neutropenia",
            "attributes": null
          },
          {
            "code": "1156403002",
            "description": "Composite Hodgkin and non-Hodgkin lymphoma",
            "attributes": null
          },
          {
            "code": "1156495004",
            "description": "Dendritic cell sarcoma",
            "attributes": null
          },
          {
            "code": "1156584007",
            "description": "X-linked intellectual disability hypotonic face syndrome",
            "attributes": null
          },
          {
            "code": "1156801007",
            "description": "Macrophage activation syndrome due to juvenile systemic onset arthritis",
            "attributes": null
          },
          {
            "code": "1157157006",
            "description": "Acute myeloid leukemia with 11q23 abnormality",
            "attributes": null
          },
          {
            "code": "1157162007",
            "description": "Intravascular large B-cell lymphoma",
            "attributes": null
          },
          {
            "code": "11603001",
            "description": "Sickle cell retinopathy",
            "attributes": null
          },
          {
            "code": "116133005",
            "description": "Congenital agammaglobulinemia",
            "attributes": null
          },
          {
            "code": "1162263002",
            "description": "Complement component 8 deficiency",
            "attributes": null
          },
          {
            "code": "1162264008",
            "description": "Malignant lymphoma of uveal tract",
            "attributes": null
          },
          {
            "code": "1162531007",
            "description": "Acute myeloid leukemia in complete remission",
            "attributes": null
          },
          {
            "code": "1162828001",
            "description": "X-linked lymphoproliferative disease due to SH2D1A deficiency",
            "attributes": null
          },
          {
            "code": "1162830004",
            "description": "X-linked lymphoproliferative disease due to XIAP deficiency",
            "attributes": null
          },
          {
            "code": "1163092001",
            "description": "Ataxia due to disorder of immune function",
            "attributes": null
          },
          {
            "code": "116691000119101",
            "description": "Marginal zone lymphoma of spleen",
            "attributes": null
          },
          {
            "code": "116811000119106",
            "description": "Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of lower limb",
            "attributes": null
          },
          {
            "code": "116821000119104",
            "description": "Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of upper limb",
            "attributes": null
          },
          {
            "code": "116841000119105",
            "description": "Marginal zone lymphoma of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "116871000119103",
            "description": "Mantle cell lymphoma of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "117211000119105",
            "description": "Peripheral T-cell lymphoma of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "1172704005",
            "description": "High grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements",
            "attributes": null
          },
          {
            "code": "1172892009",
            "description": "Autosomal recessive mendelian susceptibility to mycobacterial disease due to complete RAR related orphan receptor C receptor mutation",
            "attributes": null
          },
          {
            "code": "1172895006",
            "description": "Mendelian susceptibility to mycobacterial disease",
            "attributes": null
          },
          {
            "code": "1172966001",
            "description": "Multiple carboxylase deficiency",
            "attributes": null
          },
          {
            "code": "1173999006",
            "description": "Interleukin 21 related infantile inflammatory bowel disease",
            "attributes": null
          },
          {
            "code": "1177120001",
            "description": "Bronchiolitis obliterans syndrome following allogeneic stem cell transplant",
            "attributes": null
          },
          {
            "code": "1177173001",
            "description": "Congenital progressive bone marrow failure, B-cell immunodeficiency, skeletal dysplasia syndrome",
            "attributes": null
          },
          {
            "code": "1177175008",
            "description": "Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome",
            "attributes": null
          },
          {
            "code": "1179284005",
            "description": "Severe combined immunodeficiency due to linker for activation of T cells deficiency",
            "attributes": null
          },
          {
            "code": "1179285006",
            "description": "Combined immunodeficiency due to moesin deficiency",
            "attributes": null
          },
          {
            "code": "1179286007",
            "description": "Combined immunodeficiency due to GINS complex subunit 1 deficiency",
            "attributes": null
          },
          {
            "code": "1179288008",
            "description": "Combined immunodeficiency due to transferrin receptor deficiency",
            "attributes": null
          },
          {
            "code": "1179300002",
            "description": "B-cell expansion with nuclear factor kappa light chain enhancer of activated B cells and T-cell anergy disease",
            "attributes": null
          },
          {
            "code": "1184703009",
            "description": "Periodontitis due to infantile genetic agranulocytosis",
            "attributes": null
          },
          {
            "code": "118599009",
            "description": "Hodgkin's disease",
            "attributes": null
          },
          {
            "code": "118600007",
            "description": "Malignant lymphoma",
            "attributes": null
          },
          {
            "code": "118601006",
            "description": "Non-Hodgkin's lymphoma",
            "attributes": null
          },
          {
            "code": "118602004",
            "description": "Hodgkin's granuloma",
            "attributes": null
          },
          {
            "code": "118605002",
            "description": "Hodgkin lymphoma, nodular lymphocyte predominance",
            "attributes": null
          },
          {
            "code": "118606001",
            "description": "Hodgkin's sarcoma",
            "attributes": null
          },
          {
            "code": "118607005",
            "description": "Hodgkin lymphoma, lymphocyte-rich",
            "attributes": null
          },
          {
            "code": "118608000",
            "description": "Hodgkin's disease, nodular sclerosis",
            "attributes": null
          },
          {
            "code": "118609008",
            "description": "Hodgkin's disease, mixed cellularity",
            "attributes": null
          },
          {
            "code": "118610003",
            "description": "Hodgkin's disease, lymphocytic depletion",
            "attributes": null
          },
          {
            "code": "118611004",
            "description": "Sézary's disease",
            "attributes": null
          },
          {
            "code": "118612006",
            "description": "Malignant histiocytosis",
            "attributes": null
          },
          {
            "code": "118613001",
            "description": "Hairy cell leukemia",
            "attributes": null
          },
          {
            "code": "118614007",
            "description": "Langerhans cell histiocytosis, disseminated",
            "attributes": null
          },
          {
            "code": "118615008",
            "description": "Malignant mast cell tumor",
            "attributes": null
          },
          {
            "code": "118617000",
            "description": "Burkitt's lymphoma",
            "attributes": null
          },
          {
            "code": "118618005",
            "description": "Mycosis fungoides",
            "attributes": null
          },
          {
            "code": "1186652002",
            "description": "Inflammatory bowel disease, recurrent sinopulmonary infection syndrome",
            "attributes": null
          },
          {
            "code": "1186654001",
            "description": "Immune dysregulation, inflammatory bowel disease, arthritis, recurrent infection, lymphopenia syndrome",
            "attributes": null
          },
          {
            "code": "1186712009",
            "description": "Combined immunodeficiency due to capping protein regulator and myosin 1 linker 2 deficiency",
            "attributes": null
          },
          {
            "code": "1186714005",
            "description": "Combined immunodeficiency due to interleukin-2 inducible T cell kinase deficiency",
            "attributes": null
          },
          {
            "code": "1186715006",
            "description": "Combined immunodeficiency due to CD70 deficiency",
            "attributes": null
          },
          {
            "code": "1186719000",
            "description": "Predisposition to invasive fungal disease due to caspase recruitment domain family member 9 deficiency",
            "attributes": null
          },
          {
            "code": "1186720006",
            "description": "CCAAT enhancer binding protein epsilon-associated autoinflammation, immunodeficiency, neutrophil dysfunction syndrome",
            "attributes": null
          },
          {
            "code": "1186725001",
            "description": "Warts, immunodeficiency, lymphedema, anogenital dysplasia syndrome",
            "attributes": null
          },
          {
            "code": "1186965009",
            "description": "Periodontitis exacerbated by cyclical neutropenia",
            "attributes": null
          },
          {
            "code": "1186966005",
            "description": "Periodontitis exacerbated by familial neutropenia",
            "attributes": null
          },
          {
            "code": "1186967001",
            "description": "Periodontitis due to leukocyte adhesion deficiency",
            "attributes": null
          },
          {
            "code": "1186969003",
            "description": "Periodontitis exacerbated by acquired neutropenia",
            "attributes": null
          },
          {
            "code": "1187000005",
            "description": "Infectious mononucleosis caused by human immunodeficiency virus",
            "attributes": null
          },
          {
            "code": "1187001009",
            "description": "Infectious mononucleosis caused by human immunodeficiency virus type I",
            "attributes": null
          },
          {
            "code": "1187114007",
            "description": "Micrognathia, recurrent infections, behavioral abnormalities, mild intellectual disability syndrome",
            "attributes": null
          },
          {
            "code": "1187123005",
            "description": "Mixed phenotype acute leukemia",
            "attributes": null
          },
          {
            "code": "1187148008",
            "description": "Periodontitis exacerbated by Chédiak-Higashi syndrome",
            "attributes": null
          },
          {
            "code": "1187156006",
            "description": "Periodontitis exacerbated by human immunodeficiency virus infection",
            "attributes": null
          },
          {
            "code": "1187233008",
            "description": "Leukocyte adhesion deficiency",
            "attributes": null
          },
          {
            "code": "1187623009",
            "description": "Phosphoglucomutase 3-related congenital disorder of glycosylation",
            "attributes": null
          },
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            "description": "Susceptibility to infection due to tyrosine kinase 2 deficiency",
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            "description": "Periodontitis due to congenital neutropenia",
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            "description": "Precursor cell lymphoblastic lymphoma",
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            "description": "Lymphoproliferative disorder after transplantation of bone marrow",
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            "description": "Primary cutaneous plasmacytosis",
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            "code": "1229940001",
            "description": "Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to interleukin 7 receptor deficiency",
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            "description": "Autosomal recessive T-cell negative, B-cell positive severe combined immunodeficiency due to protein tyrosine phosphatase receptor type C deficiency",
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            "description": "Severe combined immunodeficiency due to coronin 1A deficiency",
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            "description": "Heme oxygenase-1 deficiency",
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            "description": "B-cell immunodeficiency, limb anomaly, urogenital malformation syndrome",
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            "description": "Alpha heavy chain disease, enteric form",
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            "description": "Fleckmilz",
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            "description": "Acute myeloid leukemia with BCR-ABL1",
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            "description": "Primary oculocerebral non-Hodgkin lymphoma",
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            "description": "Excision of spleen using robotic assistance",
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            "description": "Hypereosinophilic syndrome due to disease",
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            "description": "Autoimmune leukopenia",
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            "description": "Dysgammaglobulinemia",
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            "description": "Haemoglobin E beta zero thalassaemia",
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            "description": "Haemoglobin E beta plus thalassaemia",
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            "description": "Deficiency of immunoglobulin",
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            "description": "Ubiquitin specific peptidase 18 deficiency",
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            "description": "Lymphoplasmacytic lymphoma without immunoglobulin M production",
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            "description": "Hodgkin lymphoma, lymphocyte depletion of lymph nodes of neck",
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            "description": "Hodgkin lymphoma, lymphocyte depletion of lymph nodes of head and neck",
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            "description": "Hodgkin granuloma of lymph nodes of head",
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            "description": "Hodgkin granuloma of lymph nodes of neck",
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            "description": "Hodgkin granuloma of lymph nodes of head and neck",
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            "description": "Mast cell malignancy of lymph nodes of head",
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            "description": "Mast cell malignancy of lymph nodes of neck",
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            "description": "Hodgkin disease, lymphocytic-histiocytic predominance of lymph nodes of head",
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            "code": "1255738005",
            "description": "Hodgkin disease, lymphocytic-histiocytic predominance of lymph nodes of neck",
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            "code": "1255739002",
            "description": "Hodgkin disease, lymphocytic-histiocytic predominance of lymph nodes of head and neck",
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            "code": "1255740000",
            "description": "Letterer-Siwe disease of lymph nodes of head",
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            "description": "Letterer-Siwe disease of lymph nodes of neck",
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            "description": "Letterer-Siwe disease of lymph nodes of head and neck",
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            "description": "Hodgkin sarcoma of lymph nodes of head",
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            "code": "1255744009",
            "description": "Hodgkin sarcoma of lymph nodes of neck",
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            "description": "Hodgkin sarcoma of lymph nodes of head and neck",
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            "description": "Malignant histiocytosis of lymph nodes of head",
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            "description": "Malignant histiocytosis of lymph nodes of neck",
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            "description": "Malignant histiocytosis of lymph nodes of head and neck",
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            "code": "1255749004",
            "description": "Burkitt tumor of lymph nodes of head",
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            "code": "1255750004",
            "description": "Burkitt tumor of lymph nodes of neck",
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            "code": "1255751000",
            "description": "Burkitt tumor of lymph nodes of head and neck",
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            "description": "Mycosis fungoides of lymph nodes of head",
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            "description": "Mycosis fungoides of lymph nodes of neck",
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            "description": "Mycosis fungoides of lymph nodes of head and neck",
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            "description": "Hodgkin paragranuloma of lymph nodes of head",
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            "description": "Hodgkin paragranuloma of lymph nodes of neck",
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            "description": "Hodgkin paragranuloma of lymph nodes of head and neck",
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            "description": "Hodgkin disease, mixed cellularity of lymph nodes of head",
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            "description": "Hodgkin disease, mixed cellularity of lymph nodes of neck",
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            "description": "Hodgkin disease, mixed cellularity of lymph nodes of head and neck",
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            "description": "Hodgkin disease, nodular sclerosis of lymph nodes of head and neck",
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            "description": "Hodgkin disease, nodular sclerosis of lymph nodes of head",
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            "description": "Hodgkin disease, nodular sclerosis of lymph nodes of neck",
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            "description": "Malignant histiocytosis of lymph nodes of lower limb",
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            "description": "Burkitt lymphoma of lymph nodes of lower limb",
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            "description": "Hodgkin disease, nodular sclerosis of lymph nodes of lower limb",
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            "description": "Hodgkin granuloma of lymph nodes of upper limb",
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            "description": "Sézary disease of lymph nodes of head",
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            "description": "Sézary disease of lymph nodes of neck",
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            "description": "Sézary disease of lymph nodes of head and neck",
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            "description": "Hodgkin disease of lymph nodes of head",
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            "description": "Hodgkin disease of lymph nodes of neck",
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            "description": "Hodgkin disease of lymph nodes of head and neck",
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            "description": "Malignant lymphoma of lymph nodes of head",
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            "description": "Malignant lymphoma of lymph nodes of neck",
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            "description": "Malignant lymphoma of lymph nodes of head and neck",
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            "description": "Hodgkin sarcoma of lymph nodes of upper limb",
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            "description": "Malignant mast cell tumor of lymph nodes of upper limb",
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            "description": "Hodgkin disease, mixed cellularity of lymph nodes of upper limb",
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            "description": "Hodgkin disease, nodular sclerosis of lymph nodes of upper limb",
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            "description": "Letterer-Siwe disease of lymph nodes of upper limb",
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            "description": "Hodgkin disease, lymphocytic-histiocytic predominance of lymph nodes of upper limb",
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            "description": "Malignant histiocytosis of lymph nodes of upper limb",
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            "description": "Hodgkin sarcoma of lymph nodes of lower limb",
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            "description": "Letterer-Siwe disease of lymph nodes of lower limb",
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            "description": "Mycosis fungoides of lymph nodes of upper limb",
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            "description": "Hodgkin's paragranuloma of lymph nodes of lower limb",
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            "description": "Hodgkin paragranuloma of lymph nodes of upper limb",
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            "description": "Hodgkin disease, lymphocytic depletion of lymph nodes of upper limb",
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            "description": "Hodgkin disease, lymphocytic depletion of lymph nodes of lower limb",
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            "description": "Hodgkin granuloma of lymph nodes of lower limb",
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            "description": "Burkitt lymphoma of lymph nodes of upper limb",
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            "description": "Hodgkin disease, lymphocytic-histiocytic predominance of lymph nodes of lower limb",
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            "description": "Hodgkin disease, mixed cellularity of lymph nodes of lower limb",
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            "description": "Malignant mast cell tumor of lymph nodes of lower limb",
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            "description": "Hodgkin disease of lymph nodes of lower limb",
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            "description": "Hodgkin disease of lymph nodes of upper limb",
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            "description": "Malignant lymphoma of lymph nodes of upper limb",
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            "description": "Malignant lymphoma of lymph nodes of lower limb",
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            "description": "Natural killer-lymphoblastic leukemia/lymphoma",
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            "description": "Motor neuron disease due to human immunodeficiency virus infection",
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            "description": "Predisposition to severe viral infection due to interferon regulatory factor 7 deficiency",
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            "description": "Sickle cell-hemoglobin SS disease",
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            "description": "Sickle cell-beta-thalassemia",
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            "description": "Sickle cell beta plus thalassemia",
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            "description": "Sickle cell-beta^0^-thalassemia",
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            "description": "Sickle cell-delta beta^0^-thalassemia",
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            "description": "Sickle cell anemia with coexistent alpha-thalassemia",
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            "description": "Sickle cell-hemoglobin Lepore disease",
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            "description": "Sickle cell-Hemoglobin O Arab disease",
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            "description": "Hemophagocytic syndrome",
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            "description": "Malignant histiocytic disorder",
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            "description": "Malignant lymphoma of lymph nodes",
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            "description": "Chronic myelomonocytic leukemia",
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            "description": "Hypergammaglobulinemia",
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            "description": "Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial janus kinase 1 deficiency",
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            "description": "Early T-precursor lymphoblastic leukemia/lymphoma",
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            "description": "Cutaneous CD30+ lymphoproliferative disorder",
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            "description": "Biopsy of transplanted kidney",
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            "description": "Follicular lymphoma",
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            "description": "Chronic idiopathic immunoneutropenia in adult",
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            "description": "Myeloperoxidase deficiency syndrome",
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            "description": "Adult glucose-6-phosphate dehydrogenase deficiency of leukocytes syndrome",
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          {
            "code": "1297036006",
            "description": "Autosomal recessive agammaglobulinemia",
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          {
            "code": "13048006",
            "description": "Orbital lymphoma",
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          {
            "code": "13160009",
            "description": "Complication of transplanted intestines",
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          {
            "code": "133751000119102",
            "description": "Lymphoma of colon",
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          {
            "code": "13720003",
            "description": "Triclonal gammopathy",
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          {
            "code": "13886001",
            "description": "Sickle cell nephropathy",
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          {
            "code": "14024008",
            "description": "Humoral immunologic aplastic anemia",
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          {
            "code": "143291000119104",
            "description": "Non-Hodgkin lymphoma in remission",
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          {
            "code": "14333004",
            "description": "Alloimmune neonatal neutropenia",
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          {
            "code": "143551000119106",
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            "description": "Splenic vein thrombosis",
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          {
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            "description": "Granulocyte abnormality due to immune defect",
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          {
            "code": "1518005",
            "description": "Splenitis",
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            "code": "152451000119104",
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            "code": "152621000119105",
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          {
            "code": "152861000119104",
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          {
            "code": "154584000",
            "description": "Multiple myeloma etc.",
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          {
            "code": "154585004",
            "description": "Myeloma",
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          },
          {
            "code": "154781006",
            "description": "Agammaglobulinaemia &/or hypo-gammaglobulinaemia",
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          {
            "code": "155842007",
            "description": "Coeliac disease",
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          {
            "code": "161436008",
            "description": "History of leukemia",
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          {
            "code": "161626009",
            "description": "History of splenectomy",
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          {
            "code": "161668009",
            "description": "History of skin recipient",
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          {
            "code": "16294009",
            "description": "Splenomegaly",
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          {
            "code": "16318001000119107",
            "description": "Hypogammaglobulinemia due to multiple myeloma",
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          },
          {
            "code": "164165007",
            "description": "On examination - moderate splenomegaly",
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          {
            "code": "164166008",
            "description": "On examination - gross splenomegaly",
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          {
            "code": "164167004",
            "description": "On examination - painful splenomegaly",
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          {
            "code": "165816005",
            "description": "Human immunodeficiency virus detected",
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          },
          {
            "code": "1659461000000103",
            "description": "Janus kinase 2 positive polycythaemia vera",
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          {
            "code": "1659471000000105",
            "description": "Janus kinase 2 negative polycythaemia vera",
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          {
            "code": "16618004",
            "description": "Polyclonal gammopathy",
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          {
            "code": "166951000000109",
            "description": "Acute graft-versus-host disease",
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          {
            "code": "166981000000103",
            "description": "Chronic graft-versus-host disease",
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          {
            "code": "1671000",
            "description": "Sago spleen",
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          {
            "code": "16772161000119102",
            "description": "Long-term current use of vedolizumab",
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          },
          {
            "code": "16775311000119107",
            "description": "Mycosis fungoides of facial lymph node",
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          },
          {
            "code": "16894711000119103",
            "description": "Immunoglobulin G deficiency due to multiple myeloma",
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          },
          {
            "code": "17182001",
            "description": "Agranulocytosis",
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          },
          {
            "code": "17363001",
            "description": "Splenic sarcoidosis",
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          },
          {
            "code": "174691005",
            "description": "Transplantation of pancreas and duodenum",
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          },
          {
            "code": "174692003",
            "description": "Whole organ pancreatic transplant",
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          },
          {
            "code": "174693008",
            "description": "Transplantation of tail of pancreas",
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          },
          {
            "code": "174694002",
            "description": "Renewal of transplanted pancreatic tissue",
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          },
          {
            "code": "174776001",
            "description": "Total splenectomy",
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          },
          {
            "code": "174778000",
            "description": "Total splenectomy and reimplantation of fragments",
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          },
          {
            "code": "176641000000107",
            "description": "Acute graft-versus-host disease",
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          },
          {
            "code": "176651000000105",
            "description": "Chronic graft-versus-host disease",
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          },
          {
            "code": "183005",
            "description": "Autoimmune pancytopenia",
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          },
          {
            "code": "186706006",
            "description": "Human immunodeficiency virus infection constitutional disease",
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          },
          {
            "code": "186707002",
            "description": "Human immunodeficiency virus infection with neurological disease",
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          },
          {
            "code": "186708007",
            "description": "Human immunodeficiency virus infection with secondary clinical infectious disease",
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          },
          {
            "code": "186792002",
            "description": "Plasmodium vivax malaria with rupture of spleen",
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          },
          {
            "code": "187821001",
            "description": "Angiosarcoma of spleen",
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          },
          {
            "code": "187822008",
            "description": "Fibrosarcoma of spleen",
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          },
          {
            "code": "1881000119103",
            "description": "History of plasmacytoma",
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          {
            "code": "18827005",
            "description": "Complement abnormality",
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          },
          {
            "code": "188487008",
            "description": "Lymphosarcoma and reticulosarcoma",
            "attributes": null
          },
          {
            "code": "188489006",
            "description": "Reticulosarcoma of lymph nodes of head, face and neck",
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          },
          {
            "code": "188492005",
            "description": "Reticulosarcoma of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188493000",
            "description": "Reticulosarcoma of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188498009",
            "description": "Lymphosarcoma",
            "attributes": null
          },
          {
            "code": "188500005",
            "description": "Lymphosarcoma of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188501009",
            "description": "Lymphosarcoma of intrathoracic lymph nodes",
            "attributes": null
          },
          {
            "code": "188502002",
            "description": "Lymphosarcoma of intra-abdominal lymph nodes",
            "attributes": null
          },
          {
            "code": "188503007",
            "description": "Lymphosarcoma of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188504001",
            "description": "Lymphosarcoma of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188505000",
            "description": "Lymphosarcoma of intrapelvic lymph nodes",
            "attributes": null
          },
          {
            "code": "188506004",
            "description": "Lymphosarcoma of spleen",
            "attributes": null
          },
          {
            "code": "188507008",
            "description": "Lymphosarcoma of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188510001",
            "description": "Burkitt's lymphoma of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188511002",
            "description": "Burkitt's lymphoma of intrathoracic lymph nodes",
            "attributes": null
          },
          {
            "code": "188512009",
            "description": "Burkitt's lymphoma of intra-abdominal lymph nodes",
            "attributes": null
          },
          {
            "code": "188513004",
            "description": "Burkitt lymphoma of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188514005",
            "description": "Burkitt lymphoma of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188515006",
            "description": "Burkitt's lymphoma of intrapelvic lymph nodes",
            "attributes": null
          },
          {
            "code": "188516007",
            "description": "Burkitt's lymphoma of spleen",
            "attributes": null
          },
          {
            "code": "188517003",
            "description": "Burkitt's lymphoma of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188524002",
            "description": "Hodgkin's paragranuloma of intrathoracic lymph nodes",
            "attributes": null
          },
          {
            "code": "188526000",
            "description": "Hodgkin's paragranuloma of intra-abdominal lymph nodes",
            "attributes": null
          },
          {
            "code": "188529007",
            "description": "Hodgkin's paragranuloma of intrapelvic lymph nodes",
            "attributes": null
          },
          {
            "code": "188531003",
            "description": "Hodgkin's paragranuloma of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188534006",
            "description": "Hodgkin's granuloma of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188536008",
            "description": "Hodgkin's granuloma of intra-abdominal lymph nodes",
            "attributes": null
          },
          {
            "code": "188537004",
            "description": "Hodgkin's granuloma of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188538009",
            "description": "Hodgkin's granuloma of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188541000",
            "description": "Hodgkin's granuloma of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188544008",
            "description": "Hodgkin's sarcoma of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188547001",
            "description": "Hodgkin's sarcoma of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188548006",
            "description": "Hodgkin's sarcoma of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188551004",
            "description": "Hodgkin's sarcoma of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188554007",
            "description": "Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188558005",
            "description": "Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188559002",
            "description": "Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188562004",
            "description": "Hodgkin's disease, lymphocytic-histiocytic predominance of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188565002",
            "description": "Hodgkin's disease, nodular sclerosis of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188566001",
            "description": "Hodgkin's disease, nodular sclerosis of intrathoracic lymph nodes",
            "attributes": null
          },
          {
            "code": "188567005",
            "description": "Hodgkin's disease, nodular sclerosis of intra-abdominal lymph nodes",
            "attributes": null
          },
          {
            "code": "188568000",
            "description": "Hodgkin's disease, nodular sclerosis of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188569008",
            "description": "Hodgkin's disease, nodular sclerosis of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188570009",
            "description": "Hodgkin's disease, nodular sclerosis of intrapelvic lymph nodes",
            "attributes": null
          },
          {
            "code": "188572001",
            "description": "Hodgkin's disease, nodular sclerosis of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188575004",
            "description": "Hodgkin's disease, mixed cellularity of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188576003",
            "description": "Hodgkin's disease, mixed cellularity of intrathoracic lymph nodes",
            "attributes": null
          },
          {
            "code": "188577007",
            "description": "Hodgkin's disease, mixed cellularity of intra-abdominal lymph nodes",
            "attributes": null
          },
          {
            "code": "188578002",
            "description": "Hodgkin's disease, mixed cellularity of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188579005",
            "description": "Hodgkin's disease, mixed cellularity of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188580008",
            "description": "Hodgkin's disease, mixed cellularity of intrapelvic lymph nodes",
            "attributes": null
          },
          {
            "code": "188582000",
            "description": "Hodgkin's disease, mixed cellularity of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188585003",
            "description": "Hodgkin's disease, lymphocytic depletion of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188586002",
            "description": "Hodgkin's disease, lymphocytic depletion of intrathoracic lymph nodes",
            "attributes": null
          },
          {
            "code": "188587006",
            "description": "Hodgkin's disease, lymphocytic depletion of intra-abdominal lymph nodes",
            "attributes": null
          },
          {
            "code": "188589009",
            "description": "Hodgkin's disease, lymphocytic depletion of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188590000",
            "description": "Hodgkin's disease, lymphocytic depletion of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188591001",
            "description": "Hodgkin's disease, lymphocytic depletion of intrapelvic lymph nodes",
            "attributes": null
          },
          {
            "code": "188592008",
            "description": "Hodgkin's disease, lymphocytic depletion of spleen",
            "attributes": null
          },
          {
            "code": "188593003",
            "description": "Hodgkin's disease, lymphocytic depletion of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188609000",
            "description": "Nodular lymphoma of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188612002",
            "description": "Nodular lymphoma of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188613007",
            "description": "Nodular lymphoma of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188627002",
            "description": "Mycosis fungoides of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188630009",
            "description": "Sézary's disease of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188631008",
            "description": "Sézary's disease of intrathoracic lymph nodes",
            "attributes": null
          },
          {
            "code": "188632001",
            "description": "Sézary's disease of intra-abdominal lymph nodes",
            "attributes": null
          },
          {
            "code": "188633006",
            "description": "Sézary's disease of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188634000",
            "description": "Sézary's disease of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188635004",
            "description": "Sézary's disease of intrapelvic lymph nodes",
            "attributes": null
          },
          {
            "code": "188637007",
            "description": "Sézary's disease of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188640007",
            "description": "Malignant histiocytosis of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188641006",
            "description": "Malignant histiocytosis of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188642004",
            "description": "Malignant histiocytosis of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188645002",
            "description": "Leukemic reticuloendotheliosis of lymph nodes of head, face and neck",
            "attributes": null
          },
          {
            "code": "188648000",
            "description": "Leukemic reticuloendotheliosis of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188649008",
            "description": "Leukemic reticuloendotheliosis of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188660004",
            "description": "Malignant mast cell tumors",
            "attributes": null
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          {
            "code": "188662007",
            "description": "Mast cell malignancy of lymph nodes of head and neck",
            "attributes": null
          },
          {
            "code": "188663002",
            "description": "Mast cell malignancy of intrathoracic lymph nodes",
            "attributes": null
          },
          {
            "code": "188664008",
            "description": "Mast cell malignancy of intra-abdominal lymph nodes",
            "attributes": null
          },
          {
            "code": "188665009",
            "description": "Mast cell malignancy of lymph nodes of axilla and upper limb",
            "attributes": null
          },
          {
            "code": "188666005",
            "description": "Mast cell malignancy of lymph nodes of inguinal region and lower limb",
            "attributes": null
          },
          {
            "code": "188667001",
            "description": "Mast cell malignancy of intrapelvic lymph nodes",
            "attributes": null
          },
          {
            "code": "188668006",
            "description": "Malignant mast cell sarcoma of spleen",
            "attributes": null
          },
          {
            "code": "188669003",
            "description": "Mast cell malignancy of lymph nodes of multiple sites",
            "attributes": null
          },
          {
            "code": "188672005",
            "description": "Follicular non-Hodgkin's mixed small cleaved and large cell lymphoma",
            "attributes": null
          },
          {
            "code": "188674006",
            "description": "Diffuse malignant lymphoma - small non-cleaved cell",
            "attributes": null
          },
          {
            "code": "188675007",
            "description": "Malignant lymphoma - small cleaved cell",
            "attributes": null
          },
          {
            "code": "188676008",
            "description": "Malignant lymphoma - mixed small and large cell",
            "attributes": null
          },
          {
            "code": "188679001",
            "description": "Diffuse non-Hodgkin's lymphoma undifferentiated (diffuse)",
            "attributes": null
          },
          {
            "code": "188691005",
            "description": "Malignant immunoproliferative small intestinal disease",
            "attributes": null
          },
          {
            "code": "188718006",
            "description": "Malignant plasma cell neoplasm, extramedullary plasmacytoma",
            "attributes": null
          },
          {
            "code": "188721008",
            "description": "Lambda light chain myeloma",
            "attributes": null
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          {
            "code": "188725004",
            "description": "Lymphoid leukemia",
            "attributes": null
          },
          {
            "code": "188726003",
            "description": "Subacute lymphoid leukemia",
            "attributes": null
          },
          {
            "code": "188728002",
            "description": "Aleukemic lymphoid leukemia",
            "attributes": null
          },
          {
            "code": "188729005",
            "description": "Adult T-cell leukemia",
            "attributes": null
          },
          {
            "code": "188732008",
            "description": "Myeloid leukemia",
            "attributes": null
          },
          {
            "code": "188733003",
            "description": "Chronic eosinophilic leukemia",
            "attributes": null
          },
          {
            "code": "188734009",
            "description": "Chronic neutrophilic leukemia",
            "attributes": null
          },
          {
            "code": "188736006",
            "description": "Subacute myeloid leukemia",
            "attributes": null
          },
          {
            "code": "188737002",
            "description": "Chloroma",
            "attributes": null
          },
          {
            "code": "188738007",
            "description": "Granulocytic sarcoma",
            "attributes": null
          },
          {
            "code": "188741003",
            "description": "Aleukemic myeloid leukemia",
            "attributes": null
          },
          {
            "code": "188744006",
            "description": "Monocytic leukemia",
            "attributes": null
          },
          {
            "code": "188745007",
            "description": "Chronic monocytic leukemia",
            "attributes": null
          },
          {
            "code": "188746008",
            "description": "Subacute monocytic leukemia",
            "attributes": null
          },
          {
            "code": "188748009",
            "description": "Aleukemic monocytic leukemia",
            "attributes": null
          },
          {
            "code": "188754005",
            "description": "Megakaryocytic leukemia",
            "attributes": null
          },
          {
            "code": "188768003",
            "description": "Myelomonocytic leukemia",
            "attributes": null
          },
          {
            "code": "188770007",
            "description": "Subacute myelomonocytic leukemia",
            "attributes": null
          },
          {
            "code": "190030009",
            "description": "Compound leukemias",
            "attributes": null
          },
          {
            "code": "190167004",
            "description": "[X]Unspecified B-cell non-Hodgkin's lymphoma",
            "attributes": null
          },
          {
            "code": "190808009",
            "description": "Polyclonal hypergammaglobulinemia",
            "attributes": null
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          {
            "code": "190817009",
            "description": "Macroglobulinemia",
            "attributes": null
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          {
            "code": "190818004",
            "description": "Waldenström macroglobulinemia",
            "attributes": null
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            "code": "190923000",
            "description": "Sporadic primary amyloidosis",
            "attributes": null
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          {
            "code": "190955000",
            "description": "Histiocytosis X syndrome",
            "attributes": null
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          {
            "code": "190958003",
            "description": "Haemophagocytic lymphohistiocytosis",
            "attributes": null
          },
          {
            "code": "190959006",
            "description": "Hemophagocytic lymphohistiocytosis due to infection",
            "attributes": null
          },
          {
            "code": "190977001",
            "description": "(Deficiencies of humoral immunity) or (agammaglobulinemia)",
            "attributes": null
          },
          {
            "code": "190979003",
            "description": "Selective immunoglobulin A deficiency",
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          },
          {
            "code": "190980000",
            "description": "Selective immunoglobulin M deficiency",
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          },
          {
            "code": "190981001",
            "description": "Selective immunoglobulin G deficiency",
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          },
          {
            "code": "190983003",
            "description": "Hypogammaglobulinaemia: [congenital] or [agammaglobulinaemia: (Bruton's) or (congenital sex-linked & [X-linked])]",
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          },
          {
            "code": "190986006",
            "description": "Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinemia",
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            "code": "190993005",
            "description": "Autosomal recessive severe combined immunodeficiency",
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          },
          {
            "code": "190994004",
            "description": "(Severe combined immunodeficiency) or (Swiss type agammaglobulinaemia)",
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          },
          {
            "code": "190995003",
            "description": "Thymic aplasia or dysplasia with immunodeficiency",
            "attributes": null
          },
          {
            "code": "190996002",
            "description": "Severe combined immunodeficiency with reticular dysgenesis",
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          },
          {
            "code": "190997006",
            "description": "Severe combined immunodeficiency with low T- and B-cell numbers",
            "attributes": null
          },
          {
            "code": "190998001",
            "description": "Severe combined immunodeficiency with low or normal B-cell numbers",
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          {
            "code": "191001007",
            "description": "Major histocompatibility complex class I deficiency",
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          },
          {
            "code": "191002000",
            "description": "Immunodeficiency by defective expression of major histocompatibility complex class II",
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          },
          {
            "code": "191010004",
            "description": "Common variable immunodeficiency",
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          },
          {
            "code": "191011000",
            "description": "Common variable immunodeficiency with predominant abnormalities of B-cell numbers and functions",
            "attributes": null
          },
          {
            "code": "191012007",
            "description": "Common variable immunodeficiency with predominant immunoregulatory T-cell disorders",
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          },
          {
            "code": "191013002",
            "description": "Common variable immunodeficiency with autoantibodies to B- or T-cells",
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          },
          {
            "code": "191018006",
            "description": "Lymphocyte function antigen-1 defect",
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          },
          {
            "code": "191244003",
            "description": "Aplastic anemia due to chronic disease",
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          },
          {
            "code": "191246001",
            "description": "Aplastic anemia due to infection",
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          },
          {
            "code": "191247005",
            "description": "Aplastic anemia caused by radiation",
            "attributes": null
          },
          {
            "code": "191248000",
            "description": "Aplastic anemia caused by toxic cause",
            "attributes": null
          },
          {
            "code": "191256002",
            "description": "Idiopathic aplastic anemia",
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          },
          {
            "code": "191338000",
            "description": "Primary splenic neutropenia",
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          },
          {
            "code": "191345000",
            "description": "Acquired neutropenia in newborn",
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          },
          {
            "code": "191347008",
            "description": "Cyclical neutropenia",
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          },
          {
            "code": "191358004",
            "description": "Hereditary eosinophilia",
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          },
          {
            "code": "191360002",
            "description": "Drug-induced eosinophilia",
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          },
          {
            "code": "191382009",
            "description": "Chronic congestive splenomegaly",
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          },
          {
            "code": "193370005",
            "description": "Proliferative retinopathy due to sickle cell disease",
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          },
          {
            "code": "197478000",
            "description": "Congenital celiac disease",
            "attributes": null
          },
          {
            "code": "197479008",
            "description": "Acquired celiac disease",
            "attributes": null
          },
          {
            "code": "197481005",
            "description": "Celiac disease NOS",
            "attributes": null
          },
          {
            "code": "19944001",
            "description": "Autologous bone marrow transplant without purging",
            "attributes": null
          },
          {
            "code": "20224008",
            "description": "Delta heavy chain disease",
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          },
          {
            "code": "203436008",
            "description": "Osteoporosis in multiple myelomatosis",
            "attributes": null
          },
          {
            "code": "203592006",
            "description": "X-linked severe combined immunodeficiency",
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          },
          {
            "code": "205735005",
            "description": "Hypoplasia of spleen",
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          },
          {
            "code": "210180009",
            "description": "Closed injury of spleen",
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          },
          {
            "code": "21043008",
            "description": "Neutrophil cytomatrix disorder",
            "attributes": null
          },
          {
            "code": "213148006",
            "description": "Transplanted organ rejection",
            "attributes": null
          },
          {
            "code": "21527007",
            "description": "Chronic granulomatous disease, type IV",
            "attributes": null
          },
          {
            "code": "22310002",
            "description": "Chronic idiopathic monocytosis",
            "attributes": null
          },
          {
            "code": "22406001",
            "description": "Severe combined immunodeficiency due to absent lymphoid stem cells",
            "attributes": null
          },
          {
            "code": "228311000000103",
            "description": "Allograft of bone marrow from haploidentical donor",
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          },
          {
            "code": "22996003",
            "description": "Splenic infarction",
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          },
          {
            "code": "230180003",
            "description": "Human immunodeficiency virus leukoencephalopathy",
            "attributes": null
          },
          {
            "code": "230586003",
            "description": "Neuropathy due to multiple myeloma",
            "attributes": null
          },
          {
            "code": "230598008",
            "description": "Neuropathy caused by human immunodeficiency virus",
            "attributes": null
          },
          {
            "code": "23132008",
            "description": "Amyloid light-chain amyloidosis",
            "attributes": null
          },
          {
            "code": "232033003",
            "description": "Sickle cell-hemoglobin C retinopathy",
            "attributes": null
          },
          {
            "code": "232075002",
            "description": "Lymphoma of retina",
            "attributes": null
          },
          {
            "code": "23238000",
            "description": "Common variable agammaglobulinemia",
            "attributes": null
          },
          {
            "code": "23269001",
            "description": "Double heterozygous sickling disorder",
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          },
          {
            "code": "233691007",
            "description": "Asthmatic pulmonary eosinophilia",
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          },
          {
            "code": "233692000",
            "description": "Cryptogenic pulmonary eosinophilia",
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          },
          {
            "code": "234319005",
            "description": "Splenectomy",
            "attributes": null
          },
          {
            "code": "234331007",
            "description": "Syngeneic bone marrow transplant",
            "attributes": null
          },
          {
            "code": "234332000",
            "description": "Transplant of T-cell depleted allogeneic bone marrow",
            "attributes": null
          },
          {
            "code": "234333005",
            "description": "Transplant of imperfect T-cell depleted allogeneic bone marrow",
            "attributes": null
          },
          {
            "code": "234334004",
            "description": "Allogeneic related bone marrow transplant",
            "attributes": null
          },
          {
            "code": "234335003",
            "description": "Allogeneic unrelated bone marrow transplant",
            "attributes": null
          },
          {
            "code": "234367000",
            "description": "Pancytopenia with pancreatitis",
            "attributes": null
          },
          {
            "code": "234391009",
            "description": "Sickle cell anemia with high hemoglobin F",
            "attributes": null
          },
          {
            "code": "234416002",
            "description": "X-linked hypogammaglobulinemia",
            "attributes": null
          },
          {
            "code": "234417006",
            "description": "T-cell lymphocytosis",
            "attributes": null
          },
          {
            "code": "234418001",
            "description": "Chronic benign granulocytopenia",
            "attributes": null
          },
          {
            "code": "234423001",
            "description": "Chronic benign neutropenia",
            "attributes": null
          },
          {
            "code": "234424007",
            "description": "Metabolic neutropenia",
            "attributes": null
          },
          {
            "code": "234425008",
            "description": "Autoimmune neutropenia",
            "attributes": null
          },
          {
            "code": "234426009",
            "description": "Corticosteroid-induced neutrophilia",
            "attributes": null
          },
          {
            "code": "234427000",
            "description": "Monocytoid disorder",
            "attributes": null
          },
          {
            "code": "234428005",
            "description": "Lymphocytoid disorder",
            "attributes": null
          },
          {
            "code": "234429002",
            "description": "Chemotactic disorder",
            "attributes": null
          },
          {
            "code": "234430007",
            "description": "CR3-receptor deficiency",
            "attributes": null
          },
          {
            "code": "234431006",
            "description": "Specific granule deficiency",
            "attributes": null
          },
          {
            "code": "234433009",
            "description": "Myeloperoxidase deficiency",
            "attributes": null
          },
          {
            "code": "234435002",
            "description": "Hereditary hypersegmentation",
            "attributes": null
          },
          {
            "code": "234436001",
            "description": "Hemolytic erythrophagocytic syndrome",
            "attributes": null
          },
          {
            "code": "234437005",
            "description": "Hemophagocytic lymphohistiocytosis",
            "attributes": null
          },
          {
            "code": "234503004",
            "description": "Hydatid cyst of spleen caused by Echinococcus",
            "attributes": null
          },
          {
            "code": "234510005",
            "description": "Amyloidosis of spleen",
            "attributes": null
          },
          {
            "code": "234511009",
            "description": "Post-splenectomy disorder",
            "attributes": null
          },
          {
            "code": "234512002",
            "description": "Post-splenectomy thrombocytosis",
            "attributes": null
          },
          {
            "code": "234513007",
            "description": "Post-splenectomy leukocytosis",
            "attributes": null
          },
          {
            "code": "234519006",
            "description": "Bone marrow transplant rejection",
            "attributes": null
          },
          {
            "code": "234520000",
            "description": "Bone marrow transplant failure",
            "attributes": null
          },
          {
            "code": "234522008",
            "description": "Disease relapse in transplant marrow",
            "attributes": null
          },
          {
            "code": "234532001",
            "description": "Immunodeficiency disorder",
            "attributes": null
          },
          {
            "code": "234533006",
            "description": "X-linked agammaglobulinemia with growth hormone deficiency",
            "attributes": null
          },
          {
            "code": "234534000",
            "description": "Autosomal agammaglobulinemia with absent B-cells",
            "attributes": null
          },
          {
            "code": "234537007",
            "description": "Autosomal recessive hyperimmunoglobulin M syndrome",
            "attributes": null
          },
          {
            "code": "234539005",
            "description": "Immunoglobulin heavy chain deficiency",
            "attributes": null
          },
          {
            "code": "234540007",
            "description": "Selective immunoglobulin E deficiency",
            "attributes": null
          },
          {
            "code": "234541006",
            "description": "Selective immunoglobulin D deficiency",
            "attributes": null
          },
          {
            "code": "234542004",
            "description": "Selective immunoglobulin M and immunoglobulin A deficiency",
            "attributes": null
          },
          {
            "code": "234543009",
            "description": "Immunoglobulin light chain deficiency",
            "attributes": null
          },
          {
            "code": "234544003",
            "description": "Immunoglobulin subclass deficiency",
            "attributes": null
          },
          {
            "code": "234546001",
            "description": "Immunoglobulin G2 deficiency",
            "attributes": null
          },
          {
            "code": "234547005",
            "description": "Combined immunoglobulin G2 and G4 deficiency",
            "attributes": null
          },
          {
            "code": "234548000",
            "description": "Immunoglobulin G3 deficiency",
            "attributes": null
          },
          {
            "code": "234549008",
            "description": "Immunoglobulin G4 deficiency",
            "attributes": null
          },
          {
            "code": "234550008",
            "description": "Immunoglobulin G1 deficiency",
            "attributes": null
          },
          {
            "code": "234551007",
            "description": "Immunoglobulin A1 deficiency",
            "attributes": null
          },
          {
            "code": "234552000",
            "description": "Immunoglobulin A2 deficiency",
            "attributes": null
          },
          {
            "code": "234553005",
            "description": "Immunoglobulin-associated molecule deficiency",
            "attributes": null
          },
          {
            "code": "234554004",
            "description": "Secretory piece deficiency",
            "attributes": null
          },
          {
            "code": "234555003",
            "description": "Defective immunoglobulin glycosylation",
            "attributes": null
          },
          {
            "code": "234556002",
            "description": "Specific antibody deficiency",
            "attributes": null
          },
          {
            "code": "234557006",
            "description": "Anti-polysaccharide antibody deficiency",
            "attributes": null
          },
          {
            "code": "234558001",
            "description": "Anti-Haemophilus influenzae type b capsular polysaccharide antibody deficiency",
            "attributes": null
          },
          {
            "code": "234559009",
            "description": "Anti-pneumococcal polysaccharide antibody deficiency",
            "attributes": null
          },
          {
            "code": "234560004",
            "description": "Anti-meningococcal polysaccharide A antibody deficiency",
            "attributes": null
          },
          {
            "code": "234561000",
            "description": "Anti-meningococcal polysaccharide C antibody deficiency",
            "attributes": null
          },
          {
            "code": "234562007",
            "description": "Anti-protein antibody deficiency",
            "attributes": null
          },
          {
            "code": "234563002",
            "description": "Anti-staphylococcal antibody deficiency",
            "attributes": null
          },
          {
            "code": "234564008",
            "description": "Primary immunoglobulin catabolism abnormality",
            "attributes": null
          },
          {
            "code": "234565009",
            "description": "Immunoglobulin hypercatabolism",
            "attributes": null
          },
          {
            "code": "234566005",
            "description": "Familial immunoglobulin hypercatabolism",
            "attributes": null
          },
          {
            "code": "234570002",
            "description": "Severe combined immunodeficiency with maternofetal engraftment",
            "attributes": null
          },
          {
            "code": "234571003",
            "description": "Warts, hypogammaglobulinemia, infections, and myelokathexis",
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          {
            "code": "234572005",
            "description": "Benign combined immunodeficiency",
            "attributes": null
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          {
            "code": "234573000",
            "description": "Phagocytic cell defect",
            "attributes": null
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            "code": "234574006",
            "description": "Disorder of phagocytic cell number",
            "attributes": null
          },
          {
            "code": "234576008",
            "description": "Chronic familial neutropenia",
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          },
          {
            "code": "234577004",
            "description": "Lipochrome histiocytosis - familial",
            "attributes": null
          },
          {
            "code": "234578009",
            "description": "Defective phagocytic cell opsonization",
            "attributes": null
          },
          {
            "code": "234579001",
            "description": "Mannan-binding protein deficiency",
            "attributes": null
          },
          {
            "code": "234580003",
            "description": "Defective phagocytic cell chemotaxis",
            "attributes": null
          },
          {
            "code": "234581004",
            "description": "Defective phagocytic cell adhesion",
            "attributes": null
          },
          {
            "code": "234582006",
            "description": "Leukocyte adhesion deficiency - type 1",
            "attributes": null
          },
          {
            "code": "234583001",
            "description": "Leukocyte adhesion deficiency - type 2",
            "attributes": null
          },
          {
            "code": "234584007",
            "description": "Tuftsin deficiency",
            "attributes": null
          },
          {
            "code": "234585008",
            "description": "Defective phagocytic cell killing",
            "attributes": null
          },
          {
            "code": "234586009",
            "description": "Leukocyte glucose-6-phosphate dehydrogenase deficiency",
            "attributes": null
          },
          {
            "code": "234587000",
            "description": "Neutrophil lactoferrin deficiency",
            "attributes": null
          },
          {
            "code": "234588005",
            "description": "Neutrophil secondary granule deficiency",
            "attributes": null
          },
          {
            "code": "234589002",
            "description": "Glutathione synthetase deficiency",
            "attributes": null
          },
          {
            "code": "234590006",
            "description": "Gluthathione peroxidase deficiency",
            "attributes": null
          },
          {
            "code": "234591005",
            "description": "Combined phagocytic defect",
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          },
          {
            "code": "234593008",
            "description": "Classical complement pathway abnormality",
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          },
          {
            "code": "234594002",
            "description": "Complement 1q deficiency",
            "attributes": null
          },
          {
            "code": "234595001",
            "description": "Complement 1q beta chain deficiency",
            "attributes": null
          },
          {
            "code": "234596000",
            "description": "Complement 1q dysfunction",
            "attributes": null
          },
          {
            "code": "234597009",
            "description": "Complement 1r deficiency",
            "attributes": null
          },
          {
            "code": "234598004",
            "description": "Complement 1s deficiency",
            "attributes": null
          },
          {
            "code": "234599007",
            "description": "Complement 2 deficiency",
            "attributes": null
          },
          {
            "code": "234600005",
            "description": "Complement 4 deficiency",
            "attributes": null
          },
          {
            "code": "234601009",
            "description": "Complement 4A deficiency",
            "attributes": null
          },
          {
            "code": "234602002",
            "description": "Complement 4B deficiency",
            "attributes": null
          },
          {
            "code": "234603007",
            "description": "Complement 3 deficiency",
            "attributes": null
          },
          {
            "code": "234604001",
            "description": "Alternative pathway deficiency",
            "attributes": null
          },
          {
            "code": "234605000",
            "description": "Factor B deficiency",
            "attributes": null
          },
          {
            "code": "234607008",
            "description": "Factor D deficiency",
            "attributes": null
          },
          {
            "code": "234608003",
            "description": "Terminal component deficiency",
            "attributes": null
          },
          {
            "code": "234609006",
            "description": "Complement 5 deficiency",
            "attributes": null
          },
          {
            "code": "234611002",
            "description": "Complement 6 deficiency",
            "attributes": null
          },
          {
            "code": "234612009",
            "description": "Complement 7 deficiency",
            "attributes": null
          },
          {
            "code": "234613004",
            "description": "Combined complement 6 and 7 deficiencies",
            "attributes": null
          },
          {
            "code": "234614005",
            "description": "Complement 8 beta chain deficiency",
            "attributes": null
          },
          {
            "code": "234615006",
            "description": "Complement 8 beta chain dysfunction",
            "attributes": null
          },
          {
            "code": "234616007",
            "description": "Complement 8 alpha-gamma deficiency",
            "attributes": null
          },
          {
            "code": "234617003",
            "description": "Complement 9 deficiency",
            "attributes": null
          },
          {
            "code": "234618008",
            "description": "Complement regulatory factor defect",
            "attributes": null
          },
          {
            "code": "234619000",
            "description": "Hereditary C1 esterase inhibitor deficiency - deficient factor",
            "attributes": null
          },
          {
            "code": "234621005",
            "description": "Factor I deficiency",
            "attributes": null
          },
          {
            "code": "234622003",
            "description": "Factor H deficiency",
            "attributes": null
          },
          {
            "code": "234623008",
            "description": "Complement 4 binding protein deficiency",
            "attributes": null
          },
          {
            "code": "234624002",
            "description": "Decay accelerating factor deficiency",
            "attributes": null
          },
          {
            "code": "234625001",
            "description": "Homologous restriction factor deficiency",
            "attributes": null
          },
          {
            "code": "234626000",
            "description": "Complement 5a inhibitor deficiency",
            "attributes": null
          },
          {
            "code": "234627009",
            "description": "Anaphylotoxin inactivator deficiency",
            "attributes": null
          },
          {
            "code": "234628004",
            "description": "Complement receptor deficiency",
            "attributes": null
          },
          {
            "code": "234629007",
            "description": "Complement receptor 1 deficiency",
            "attributes": null
          },
          {
            "code": "234630002",
            "description": "Complement receptor 3 deficiency",
            "attributes": null
          },
          {
            "code": "234631003",
            "description": "Immunodeficiency with major anomalies",
            "attributes": null
          },
          {
            "code": "234632005",
            "description": "Immunodeficiency associated with chromosomal abnormality",
            "attributes": null
          },
          {
            "code": "234633000",
            "description": "Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency",
            "attributes": null
          },
          {
            "code": "234634006",
            "description": "Chromosome 18 syndromes and antibody deficiency",
            "attributes": null
          },
          {
            "code": "234635007",
            "description": "Chromosome 22 abnormalities with hypogammaglobulinemia",
            "attributes": null
          },
          {
            "code": "234636008",
            "description": "Monosomy 22 and absence of immunoglobulin A",
            "attributes": null
          },
          {
            "code": "234637004",
            "description": "Deletion of X-chromosome and hypogammaglobulinemia",
            "attributes": null
          },
          {
            "code": "234638009",
            "description": "Microcephaly, normal intelligence and immunodeficiency",
            "attributes": null
          },
          {
            "code": "234639001",
            "description": "Triple X syndrome, epilepsy, and hypogammaglobulinemia",
            "attributes": null
          },
          {
            "code": "234640004",
            "description": "18-p syndrome with associated immunodeficiency",
            "attributes": null
          },
          {
            "code": "234641000",
            "description": "Immunodeficiency associated with multiple organ system abnormalities",
            "attributes": null
          },
          {
            "code": "234646005",
            "description": "Graft-versus-host disease",
            "attributes": null
          },
          {
            "code": "235009000",
            "description": "Human immunodeficiency virus-associated periodontitis",
            "attributes": null
          },
          {
            "code": "235726002",
            "description": "Human immunodeficiency virus enteropathy",
            "attributes": null
          },
          {
            "code": "236406007",
            "description": "Acquired immune deficiency syndrome-related nephropathy",
            "attributes": null
          },
          {
            "code": "236512004",
            "description": "Leukemic infiltrate of kidney",
            "attributes": null
          },
          {
            "code": "236513009",
            "description": "Lymphoma of kidney",
            "attributes": null
          },
          {
            "code": "236585005",
            "description": "De novo transplant disease",
            "attributes": null
          },
          {
            "code": "23719005",
            "description": "Transplantation of bone marrow",
            "attributes": null
          },
          {
            "code": "23761004",
            "description": "Hyposplenism",
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            "code": "237865009",
            "description": "Primary amyloidosis of light chain type",
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            "code": "237926007",
            "description": "Glutathione synthase deficiency without 5-oxoprolinuria",
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            "code": "23829007",
            "description": "Celiac disease",
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          {
            "code": "238931006",
            "description": "Eosinophilic cellulitis",
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          {
            "code": "240103002",
            "description": "Human immunodeficiency virus myopathy",
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          {
            "code": "240531002",
            "description": "African Burkitt's lymphoma",
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          {
            "code": "240630008",
            "description": "Hyperreactive malarial splenomegaly syndrome",
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          {
            "code": "240794006",
            "description": "Splenic schistosomal giant cell lymphoma",
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            "code": "24159007",
            "description": "Persistent lymphocytosis",
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            "code": "24181002",
            "description": "Aplasia of thymus gland with immunodeficiency",
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            "code": "24419001",
            "description": "Disorder of complement",
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            "code": "24743004",
            "description": "Complement deficiency disease",
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          {
            "code": "247860002",
            "description": "Familial neutropenia",
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          {
            "code": "24829000",
            "description": "Eosinophilic ulcerative colitis",
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          },
          {
            "code": "248693006",
            "description": "Chronic idiopathic neutropenia",
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          },
          {
            "code": "24974008",
            "description": "Myelokathexis",
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          {
            "code": "24975009",
            "description": "Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin",
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            "code": "25050002",
            "description": "Alpha heavy chain disease, respiratory form",
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          {
            "code": "25109007",
            "description": "Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome",
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          {
            "code": "254067002",
            "description": "Immuno-osseous dysplasia",
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          {
            "code": "254289008",
            "description": "Post-transplant neoplasia",
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          {
            "code": "254290004",
            "description": "Lymphoproliferative disorder following transplantation",
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          {
            "code": "25472008",
            "description": "Sickle cell-hemoglobin D disease",
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          {
            "code": "254792006",
            "description": "Proliferating angioendotheliomatosis",
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          {
            "code": "25502009",
            "description": "Episodic lymphocytopenia",
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          {
            "code": "255101006",
            "description": "Sézary disease of skin",
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          },
          {
            "code": "255102004",
            "description": "Angioendotheliomatosis",
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          {
            "code": "255191003",
            "description": "Localized malignant reticulohistiocytoma",
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          {
            "code": "26252007",
            "description": "Chronic granulomatous disease, type IIA",
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          },
          {
            "code": "262819007",
            "description": "Intraparenchymal hematoma of spleen",
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          },
          {
            "code": "262821002",
            "description": "Avulsion of spleen",
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          {
            "code": "262823004",
            "description": "Capsular tear of spleen",
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          {
            "code": "2631000119108",
            "description": "History of bone marrow transplant",
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          {
            "code": "263661007",
            "description": "Complement 5 dysfunction",
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          {
            "code": "266478000",
            "description": "Coeliac disease",
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          {
            "code": "267440005",
            "description": "Monoclonal paraproteinemia",
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          {
            "code": "267460002",
            "description": "Congenital hypogammaglobulinemia",
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          {
            "code": "267512002",
            "description": "Agammaglobulinaemia &/or hypo-gammaglobulinaemia",
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          {
            "code": "267524009",
            "description": "Constitutional aplastic anemia with malformation",
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          },
          {
            "code": "267527002",
            "description": "Aplastic anemia due to drugs",
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          {
            "code": "267538002",
            "description": "Agranulocytopenic disorder",
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          {
            "code": "267540007",
            "description": "Neutropenia caused by ionizing radiation",
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          },
          {
            "code": "267543009",
            "description": "Functional disorders of polymorphonuclear neutrophils",
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          },
          {
            "code": "269295009",
            "description": "Transplanted organ failure",
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          {
            "code": "269475001",
            "description": "Malignant neoplasm of lymphoid, hematopoietic and/or related tissue",
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          {
            "code": "269476000",
            "description": "Nodular lymphoma",
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            "code": "269629004",
            "description": "Multiple myeloma etc.",
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          {
            "code": "27254001",
            "description": "Extramedullary hematopoiesis of spleen",
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            "code": "274593002",
            "description": "[EDTA] Myelomatosis associated with renal failure",
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          },
          {
            "code": "274905008",
            "description": "Malignant lymphoma - lymphocytic, intermediate differentiation",
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            "code": "275404008",
            "description": "Celiac rickets",
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          {
            "code": "275523003",
            "description": "Pancytopenia-dysmelia",
            "attributes": null
          },
          {
            "code": "275524009",
            "description": "Immunoproliferative neoplasm",
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            "code": "276576000",
            "description": "Neutropenia of the small for gestational age baby",
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          {
            "code": "276665006",
            "description": "Congenital acquired immune deficiency syndrome",
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          {
            "code": "276666007",
            "description": "Congenital human immunodeficiency virus positive status syndrome",
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          {
            "code": "276811008",
            "description": "Gastric lymphoma",
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            "code": "276815004",
            "description": "Lymphoma of intestine",
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            "code": "276836002",
            "description": "Primary cerebral lymphoma",
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            "code": "277451006",
            "description": "Part organ pancreatic transplant",
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            "code": "277466009",
            "description": "Lymphoproliferative disorder",
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            "code": "277473004",
            "description": "B-cell chronic lymphocytic leukemia",
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          {
            "code": "277474005",
            "description": "B-cell chronic lymphocytic leukemia variant",
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          {
            "code": "277543005",
            "description": "Malignant white blood cell disorder",
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          {
            "code": "277545003",
            "description": "T-cell chronic lymphocytic leukemia",
            "attributes": null
          },
          {
            "code": "277549009",
            "description": "Chronic lymphocytic prolymphocytic leukemia syndrome",
            "attributes": null
          },
          {
            "code": "277550009",
            "description": "Richter's syndrome",
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          {
            "code": "277551008",
            "description": "Splenic lymphoma with villous lymphocytes",
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          },
          {
            "code": "277567002",
            "description": "T-cell prolymphocytic leukemia",
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            "code": "277568007",
            "description": "Hairy cell leukemia variant",
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          {
            "code": "277569004",
            "description": "Large granular lymphocytic leukemia",
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            "code": "277570003",
            "description": "Lymphoma with spill",
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            "code": "277571004",
            "description": "B-cell acute lymphoblastic leukemia",
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          {
            "code": "277572006",
            "description": "Precursor B-cell acute lymphoblastic leukemia",
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            "code": "277573001",
            "description": "Common acute lymphoblastic leukemia",
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          {
            "code": "277574007",
            "description": "Null cell acute lymphoblastic leukemia",
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            "code": "277575008",
            "description": "T-lymphoblastic leukemia",
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            "description": "Monoclonal gammopathy of uncertain significance",
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            "code": "277579002",
            "description": "Light chain myeloma",
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            "description": "Non-secretory myeloma",
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            "code": "277587001",
            "description": "Juvenile chronic myeloid leukemia",
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            "description": "Myelodysplastic-myeloproliferative neoplasm with neutrophilia",
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            "code": "277601005",
            "description": "Acute monoblastic leukemia",
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            "code": "277602003",
            "description": "Acute megakaryoblastic leukemia",
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            "description": "Malignant myeloid-lymphoid neoplasm",
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            "description": "Hodgkin's disease, lymphocytic predominance - diffuse",
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            "description": "Hodgkin's disease, nodular sclerosis - lymphocytic predominance",
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            "description": "Hodgkin's disease, nodular sclerosis - mixed cellularity",
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            "description": "Hodgkin's disease, nodular sclerosis - lymphocytic depletion",
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            "description": "Cutaneous peripheral T-cell lymphoma",
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            "description": "Prethymic and thymic T-cell lymphoma/leukemia",
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            "code": "277615007",
            "description": "Low grade B-cell lymphoma",
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            "description": "Diffuse low grade B-cell lymphoma",
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            "code": "277617004",
            "description": "High grade B-cell lymphoma",
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            "code": "277618009",
            "description": "Follicular low grade B-cell lymphoma",
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            "code": "277619001",
            "description": "B-cell prolymphocytic leukemia",
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            "code": "277622004",
            "description": "Mucosa-associated lymphoma",
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            "description": "Monocytoid B-cell lymphoma",
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            "code": "277624003",
            "description": "Follicular malignant lymphoma - mixed cell type",
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            "code": "277625002",
            "description": "Follicular malignant lymphoma - small cleaved cell",
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            "code": "277626001",
            "description": "Diffuse high grade B-cell lymphoma",
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            "description": "Nodular high grade B-cell lymphoma",
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            "code": "277628000",
            "description": "Diffuse malignant lymphoma - large cleaved cell",
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            "code": "277629008",
            "description": "Diffuse malignant lymphoma - large non-cleaved cell",
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            "description": "Diffuse malignant lymphoma - centroblastic polymorphic",
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            "code": "277637000",
            "description": "Large cell anaplastic lymphoma",
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            "description": "Follicular malignant lymphoma - large cell",
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            "code": "277642008",
            "description": "Low grade T-cell lymphoma",
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            "code": "277643003",
            "description": "High grade T-cell lymphoma",
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            "description": "Peripheral T-cell lymphoma - pleomorphic small cell",
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            "description": "Peripheral T-cell lymphoma - pleomorphic medium and large cell",
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            "description": "Enteropathy-associated T-cell lymphoma",
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            "description": "Malignant lymphoma of thyroid gland",
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            "description": "Malignant lymphoma of breast",
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            "description": "Hypergranular promyelocytic leukemia",
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            "description": "Acute biphenotypic leukemia",
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            "description": "Human immunodeficiency virus-related sclerosing cholangitis",
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            "description": "Immunoglobulin A myeloma",
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            "description": "Immunoglobulin G myeloma",
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            "description": "Immunoglobulin D myeloma",
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            "description": "Immunoglobulin A monoclonal gammopathy of uncertain significance",
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            "description": "Immunoglobulin G monoclonal gammopathy of uncertain significance",
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            "description": "Immunoglobulin M monoclonal gammopathy of uncertain significance",
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            "description": "Immunoglobulin D monoclonal gammopathy of uncertain significance",
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            "description": "Light chain monoclonal gammopathy of uncertain significance",
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            "description": "Metastasis to spleen of unknown primary",
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            "description": "Acute promyelocytic leukemia - hypogranular variant",
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            "description": "Intermediate grade B-cell lymphoma",
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            "description": "Acute myelomonocytic leukemia - eosinophilic variant",
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            "description": "Thymus transplantation",
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            "description": "Granulation anomaly",
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            "description": "Granulocyte granule deficiency",
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            "description": "Constitutional aplastic anemia",
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            "description": "Eosinophilic colitis",
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            "description": "Immunoglobulin A deficiency",
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            "description": "Chronic granulomatous disease, type I",
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            "description": "Spleen absent",
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            "description": "Malignant lymphoma - small lymphocytic",
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            "description": "Diffuse malignant lymphoma - centroblastic",
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            "description": "Nodular malignant lymphoma, lymphocytic - well differentiated",
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            "description": "Nodular malignant lymphoma, lymphocytic - intermediate differentiation",
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            "description": "Subacute leukemia",
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            "description": "Aleukemic leukemia",
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            "description": "Phagocytic cell dysfunction",
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            "description": "Hereditary splenic hypoplasia",
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            "description": "Malignant lymphoma, convoluted cell type",
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            "description": "Malignant lymphoma, follicular center cell",
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            "description": "Malignant lymphoma, follicular center cell, cleaved",
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            "description": "Malignant lymphoma, follicular center cell, non-cleaved",
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            "description": "Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency",
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            "description": "Aplastic anemia",
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            "description": "Monosomy 7 syndrome",
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            "description": "Atypical hairy cell leukemia",
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            "description": "Malignant mastocytosis",
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            "description": "Basophilic leukemia",
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            "description": "Neutrophilic leukemia",
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            "description": "Malignant lymphoma - lymphoplasmacytic",
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            "description": "Diffuse malignant lymphoma - centroblastic-centrocytic",
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            "description": "Malignant lymphoma - centrocytic",
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            "description": "Hodgkin's disease, lymphocytic depletion, diffuse fibrosis",
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            "description": "Hodgkin's disease, lymphocytic depletion, reticular type",
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            "description": "Hodgkin's disease, nodular sclerosis - cellular phase",
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            "description": "Malignant lymphoma, mixed lymphocytic-histiocytic, nodular",
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            "description": "Malignant lymphoma, centroblastic-centrocytic, follicular",
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            "description": "Malignant lymphoma, lymphocytic, poorly differentiated, nodular",
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            "description": "Malignant lymphoma, centroblastic type, follicular",
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            "description": "Microglioma",
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            "description": "Histiocytic medullary reticulosis",
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            "description": "Primary myelofibrosis",
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            "description": "Follicular lymphoma",
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            "description": "Secondary eosinophilia",
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            "description": "Lymphomatoid papulosis",
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            "description": "Solid organ transplant to recipient",
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            "description": "Severe combined immunodeficiency disease",
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            "description": "Lambda light chain myeloma",
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            "description": "Laparoscopic total splenectomy",
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            "description": "Leukemic infiltrate of choroid",
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            "description": "Leukemic infiltrate of retina",
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            "description": "Aseptic meningitis due to human immunodeficiency virus infection",
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            "description": "Granulocytosis",
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            "description": "Qualitative abnormality of granulocyte",
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            "description": "Idiopathic eosinophilia",
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            "description": "Toxic neutropenia",
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            "description": "Lymphocyte disorder",
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            "description": "Familial hemophagocytic lymphohistiocytosis",
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            "description": "Distal subtotal pancreatectomy with splenectomy and pancreaticojejunostomy",
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            "code": "3439009",
            "description": "Severe combined immunodeficiency due to absent peripheral T cell maturation",
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            "code": "34916006",
            "description": "Neutrophil motility disorder",
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            "code": "350353007",
            "description": "De Vaal's syndrome",
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            "description": "B-cell lymphoma of intra-abdominal lymph nodes",
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            "description": "B-cell lymphoma of lymph nodes of multiple sites",
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            "description": "Reticular dysgenesis with congenital aleukocytosis",
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            "description": "Small lymphocytic B-cell lymphoma of lymph nodes of multiple sites",
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            "description": "Small lymphocytic B-cell lymphoma of intra-abdominal lymph nodes",
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            "description": "Non-Hodgkin's lymphoma of lymph nodes of multiple sites",
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            "description": "Extramedullary plasmacytoma in remission",
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            "description": "Sickle cell-hemoglobin C disease",
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            "description": "Acute myeloid leukemia, minimal differentiation, FAB M0",
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            "description": "Acute myeloid leukemia without maturation, FAB M1",
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          {
            "code": "359648001",
            "description": "Acute myeloid leukemia with maturation, FAB M2",
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            "code": "36070007",
            "description": "Wiskott-Aldrich syndrome",
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            "code": "361194002",
            "description": "Perinatal pulmonary fibroplasia",
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            "code": "361195001",
            "description": "Pulmonary fibroplasia",
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          {
            "code": "36138009",
            "description": "Congenital immunodeficiency disease",
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            "code": "362993009",
            "description": "Autosomal recessive severe combined immunodeficiency disease",
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            "description": "Complement component deficiency",
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          {
            "code": "363040003",
            "description": "Congenital immunodeficiency involving the hematopoietic system",
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          },
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            "description": "Hereditary disorder of immune system",
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          },
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            "code": "363265005",
            "description": "Predominant humoral immune deficiency",
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            "code": "363499005",
            "description": "Malignant neoplasm of spleen",
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            "code": "36472007",
            "description": "Sickle cell-thalassemia disease",
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          {
            "code": "36752001",
            "description": "Congenital splenomegaly",
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          {
            "code": "36760000",
            "description": "Hepatosplenomegaly",
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          {
            "code": "36980009",
            "description": "Severe combined immunodeficiency due to absent adenosine deaminase",
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            "code": "371012000",
            "description": "Acute lymphoblastic leukemia, transitional pre-B-cell",
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          {
            "code": "371134001",
            "description": "Malignant lymphoma, large cell, polymorphous, immunoblastic",
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          {
            "code": "37465004",
            "description": "Plasmacytosis",
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          {
            "code": "37548006",
            "description": "Hypopigmentation-immunodeficiency disease",
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          {
            "code": "378841000000102",
            "description": "Allograft of bone marrow from unmatched unrelated donor",
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            "code": "38064006",
            "description": "Reactive monocytosis",
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          {
            "code": "38096003",
            "description": "Functional asplenia",
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          {
            "code": "387759001",
            "description": "Chronic granulomatous disease",
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          },
          {
            "code": "38970002",
            "description": "Doan-Wright syndrome",
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          {
            "code": "3902000",
            "description": "Non dose-related drug-induced neutropenia",
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          },
          {
            "code": "39112005",
            "description": "Glutathione synthase deficiency with 5-oxoprolinuria",
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          {
            "code": "396330006",
            "description": "Celiac crisis",
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          },
          {
            "code": "396331005",
            "description": "Celiac disease",
            "attributes": null
          },
          {
            "code": "39674000",
            "description": "Familial C3B inhibitor deficiency syndrome",
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          },
          {
            "code": "397008008",
            "description": "Aggressive lymphadenopathic mastocytosis with eosinophilia",
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          },
          {
            "code": "397009000",
            "description": "Mast cell malignancy",
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          {
            "code": "397011009",
            "description": "Mast cell malignancy of lymph nodes",
            "attributes": null
          },
          {
            "code": "397015000",
            "description": "Systemic mastocytosis with associated clonal hematological non-mast cell lineage disease",
            "attributes": null
          },
          {
            "code": "397016004",
            "description": "Systemic mast cell disease",
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          },
          {
            "code": "397763006",
            "description": "Human immunodeficiency virus encephalopathy",
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          },
          {
            "code": "39795003",
            "description": "Hand-Schüller-Christian disease",
            "attributes": null
          },
          {
            "code": "398055000",
            "description": "T-lymphocyte deficiency",
            "attributes": null
          },
          {
            "code": "398250003",
            "description": "Familial hemophagocytic lymphohistiocytosis",
            "attributes": null
          },
          {
            "code": "398329009",
            "description": "Human immunodeficiency virus encephalitis",
            "attributes": null
          },
          {
            "code": "398623004",
            "description": "Myelodysplastic syndrome with excess blasts",
            "attributes": null
          },
          {
            "code": "400001003",
            "description": "Primary cutaneous lymphoma",
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          },
          {
            "code": "400122007",
            "description": "Primary cutaneous T-cell lymphoma",
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          },
          {
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            "description": "History of acute leukemia",
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          {
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            "description": "[X]Unspecified B-cell non-Hodgkin's lymphoma",
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          {
            "code": "40145002",
            "description": "Congenital neutrophil actin dysfunction",
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          {
            "code": "40197009",
            "description": "Chronic granulomatous disease, type IA",
            "attributes": null
          },
          {
            "code": "402355000",
            "description": "Acute graft-versus-host disease",
            "attributes": null
          },
          {
            "code": "402356004",
            "description": "Chronic graft-versus-host disease",
            "attributes": null
          },
          {
            "code": "402357008",
            "description": "Lichenoid chronic graft-versus-host disease",
            "attributes": null
          },
          {
            "code": "402358003",
            "description": "Sclerodermoid chronic graft-versus-host disease",
            "attributes": null
          },
          {
            "code": "402359006",
            "description": "Toxic epidermal necrolysis due to graft-versus-host disease",
            "attributes": null
          },
          {
            "code": "402360001",
            "description": "Materno-fetal graft-versus-host disease",
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          },
          {
            "code": "402361002",
            "description": "Nail dystrophy due to graft-versus-host disease",
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          },
          {
            "code": "402362009",
            "description": "Oral mucosal disease due to graft-versus-host disease",
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          },
          {
            "code": "402415001",
            "description": "Schnitzler syndrome",
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          },
          {
            "code": "402416000",
            "description": "Urticarial vasculitis with monoclonal immunoglobulin M component, Schnitzler",
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          },
          {
            "code": "402453006",
            "description": "Amyloid light chain amyloidosis due to multiple myeloma",
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          },
          {
            "code": "402454000",
            "description": "Primary systemic amyloidosis due to occult plasma cell dyscrasia",
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          },
          {
            "code": "402483002",
            "description": "Immunodeficiency with multicarboxylase deficiency",
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          {
            "code": "402791005",
            "description": "B-lymphocyte immunodeficiency",
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          {
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            "description": "T-lymphocyte immunodeficiency",
            "attributes": null
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          {
            "code": "402793008",
            "description": "Heritable disorder of neutrophil production",
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          {
            "code": "402794002",
            "description": "Heritable disorder of neutrophil function",
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          {
            "code": "402879006",
            "description": "T-cell leukemic infiltration of skin",
            "attributes": null
          },
          {
            "code": "402880009",
            "description": "Primary cutaneous large T-cell lymphoma",
            "attributes": null
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          {
            "code": "402881008",
            "description": "Primary cutaneous B-cell lymphoma",
            "attributes": null
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          {
            "code": "402882001",
            "description": "Hodgkin's disease affecting skin",
            "attributes": null
          },
          {
            "code": "402901009",
            "description": "Oral hairy leukoplakia associated with human immunodeficiency virus disease",
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          {
            "code": "403735006",
            "description": "Eosinophilia-myalgia syndrome from tryptophan",
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          },
          {
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            "description": "X-linked hyper-immunoglobulin M syndrome",
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          },
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            "description": "Autosomal recessive hyperimmunoglobulin M syndrome",
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            "description": "Wiskott-Aldrich autosomal dominant variant syndrome",
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            "description": "Jung syndrome",
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          {
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            "description": "Siccardi syndrome",
            "attributes": null
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          {
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            "description": "Lymphomatoid papulosis type A (CD-30 positive type)",
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          {
            "code": "404104001",
            "description": "Lymphomatoid papulosis type B - mycosis fungoides-like",
            "attributes": null
          },
          {
            "code": "404105000",
            "description": "Lymphomatoid papulosis type C (anaplastic large-cell lymphoma-like)",
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          {
            "code": "404106004",
            "description": "Lymphomatoid papulosis with Hodgkin's disease",
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          {
            "code": "404107008",
            "description": "Patch/plaque stage mycosis fungoides",
            "attributes": null
          },
          {
            "code": "404108003",
            "description": "Poikilodermatous mycosis fungoides",
            "attributes": null
          },
          {
            "code": "404109006",
            "description": "Follicular mucinosis type mycosis fungoides",
            "attributes": null
          },
          {
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            "description": "Hypomelanotic mycosis fungoides",
            "attributes": null
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          {
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            "description": "Lymphomatoid papulosis-associated mycosis fungoides",
            "attributes": null
          },
          {
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            "description": "Granulomatous mycosis fungoides",
            "attributes": null
          },
          {
            "code": "404113004",
            "description": "Tumor stage mycosis fungoides",
            "attributes": null
          },
          {
            "code": "404114005",
            "description": "Erythrodermic mycosis fungoides",
            "attributes": null
          },
          {
            "code": "404115006",
            "description": "Bullous mycosis fungoides",
            "attributes": null
          },
          {
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            "description": "Mycosis fungoides with systemic infiltration",
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          },
          {
            "code": "404117003",
            "description": "Spongiotic mycosis fungoides",
            "attributes": null
          },
          {
            "code": "404118008",
            "description": "Syringotropic mycosis fungoides",
            "attributes": null
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          {
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            "description": "Pagetoid reticulosis",
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          {
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            "description": "Localized pagetoid reticulosis",
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          {
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            "description": "Generalized pagetoid reticulosis",
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          {
            "code": "404122003",
            "description": "Leukemic infiltration of skin (chronic T-cell lymphocytic leukemia)",
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          {
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            "description": "Leukemic infiltration of skin (T-cell prolymphocytic leukemia)",
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          },
          {
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            "description": "Leukemic infiltration of skin (T-cell lymphoblastic leukemia)",
            "attributes": null
          },
          {
            "code": "404125001",
            "description": "CD-30 positive anaplastic large T-cell cutaneous lymphoma",
            "attributes": null
          },
          {
            "code": "404126000",
            "description": "CD-30 positive pleomorphic large T-cell cutaneous lymphoma",
            "attributes": null
          },
          {
            "code": "404127009",
            "description": "CD-30 positive T-immunoblastic cutaneous lymphoma",
            "attributes": null
          },
          {
            "code": "404128004",
            "description": "CD-30 negative cutaneous T-cell lymphoma",
            "attributes": null
          },
          {
            "code": "404129007",
            "description": "CD-30 negative anaplastic large T-cell cutaneous lymphoma",
            "attributes": null
          },
          {
            "code": "404130002",
            "description": "CD-30 negative pleomorphic large T-cell cutaneous lymphoma",
            "attributes": null
          },
          {
            "code": "404131003",
            "description": "CD-30 negative T-immunoblastic cutaneous lymphoma",
            "attributes": null
          },
          {
            "code": "404132005",
            "description": "Pleomorphic small/medium-sized cell cutaneous T-cell lymphoma",
            "attributes": null
          },
          {
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            "description": "Subcutaneous panniculitic cutaneous T-cell lymphoma",
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          },
          {
            "code": "404134006",
            "description": "Anaplastic large T-cell systemic malignant lymphoma",
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          },
          {
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            "description": "Angiocentric natural killer cell and T-cell malignant lymphoma involving skin",
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          {
            "code": "404136008",
            "description": "Aggressive natural killer-cell leukemia involving skin",
            "attributes": null
          },
          {
            "code": "404137004",
            "description": "Precursor B-cell lymphoblastic lymphoma involving skin",
            "attributes": null
          },
          {
            "code": "404138009",
            "description": "Small lymphocytic B-cell lymphoma involving skin",
            "attributes": null
          },
          {
            "code": "404139001",
            "description": "Leukemic infiltration of skin in hairy-cell leukemia",
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          },
          {
            "code": "404140004",
            "description": "Primary cutaneous marginal zone B-cell lymphoma",
            "attributes": null
          },
          {
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            "description": "Primary cutaneous immunocytoma",
            "attributes": null
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          {
            "code": "404142007",
            "description": "Primary cutaneous plasmacytoma",
            "attributes": null
          },
          {
            "code": "404143002",
            "description": "Primary cutaneous follicular center B-cell lymphoma",
            "attributes": null
          },
          {
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            "description": "Primary cutaneous diffuse large cell B-cell lymphoma",
            "attributes": null
          },
          {
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            "description": "Primary cutaneous anaplastic large cell B-cell lymphoma",
            "attributes": null
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          {
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            "description": "Primary cutaneous diffuse large cell B-cell lymphoma of the leg",
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          {
            "code": "404147001",
            "description": "Follicular center B-cell lymphoma (nodal/systemic with skin involvement)",
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          },
          {
            "code": "404148006",
            "description": "Diffuse large B-cell lymphoma (nodal/systemic with skin involvement)",
            "attributes": null
          },
          {
            "code": "404149003",
            "description": "Lymphoplasmacytic B-cell lymphoma, nodal/systemic with skin involvement",
            "attributes": null
          },
          {
            "code": "404150003",
            "description": "Mantle cell B-cell lymphoma (nodal/systemic with skin involvement)",
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          {
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            "description": "Leukemic infiltration of skin in myeloid leukemia",
            "attributes": null
          },
          {
            "code": "404152006",
            "description": "Leukemic infiltration of skin in acute myeloid leukemia",
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          },
          {
            "code": "404153001",
            "description": "Leukemic infiltration of skin in chronic myeloid leukemia",
            "attributes": null
          },
          {
            "code": "404154007",
            "description": "Leukemic infiltration of skin in monocytic leukemia",
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          {
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            "description": "Granulocytic sarcoma affecting skin",
            "attributes": null
          },
          {
            "code": "404156009",
            "description": "Leukemic infiltration of skin",
            "attributes": null
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          {
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            "description": "Specific skin infiltration in Hodgkin's disease",
            "attributes": null
          },
          {
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            "description": "Necrobiotic xanthogranuloma with paraproteinemia",
            "attributes": null
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          {
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            "description": "Malignant histiocytosis involving skin",
            "attributes": null
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          {
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            "description": "Mast cell leukemia affecting skin",
            "attributes": null
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          {
            "code": "405631006",
            "description": "Pediatric human immunodeficiency virus infection",
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          {
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            "description": "CD4 T lymphocyte deficiency",
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          {
            "code": "40780007",
            "description": "Human immunodeficiency virus I infection",
            "attributes": null
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          {
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            "description": "Febrile neutropenia",
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          {
            "code": "413389003",
            "description": "Accelerated phase chronic myeloid leukemia",
            "attributes": null
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          {
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            "description": "Acute monocytic leukemia",
            "attributes": null
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          {
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            "description": "Acute monocytic/monoblastic leukemia",
            "attributes": null
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          {
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            "description": "Angioimmunoblastic T-cell lymphoma",
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            "description": "Aplastic anemia associated with metabolic alteration",
            "attributes": null
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          {
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            "description": "Aplastic anemia associated with pancreatitis",
            "attributes": null
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          {
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            "description": "Aplastic anemia associated with pregnancy",
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          {
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            "description": "Smoldering myeloma",
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          {
            "code": "413656006",
            "description": "Blastic phase chronic myeloid leukemia",
            "attributes": null
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          {
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            "description": "Chronic disease of immune function",
            "attributes": null
          },
          {
            "code": "413842007",
            "description": "Chronic myeloid leukemia in lymphoid blast crisis",
            "attributes": null
          },
          {
            "code": "413843002",
            "description": "Chronic myeloid leukemia in myeloid blast crisis",
            "attributes": null
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            "description": "Chronic phase chronic myeloid leukemia",
            "attributes": null
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            "description": "Disorder of immune function",
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          {
            "code": "414166008",
            "description": "Natural Killer cell and T-cell malignant lymphoma nasal type",
            "attributes": null
          },
          {
            "code": "414376003",
            "description": "Hairy leukoplakia of tongue associated with human immunodeficiency virus disease",
            "attributes": null
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          {
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            "description": "Hereditary white blood cell disorder",
            "attributes": null
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          {
            "code": "414553000",
            "description": "Kappa light chain myeloma",
            "attributes": null
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          {
            "code": "414604009",
            "description": "Leukoplakia of tongue associated with human immunodeficiency virus disease",
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          {
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            "description": "Mucosa-associated lymphoid tissue lymphoma of orbit",
            "attributes": null
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            "description": "Multiple solitary plasmacytomas",
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          {
            "code": "414850009",
            "description": "Neutrophilia disorder",
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          {
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            "description": "Panleukopenia",
            "attributes": null
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          {
            "code": "415110002",
            "description": "Plasma cell myeloma/plasmacytoma",
            "attributes": null
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          {
            "code": "415112005",
            "description": "Plasmacytoma",
            "attributes": null
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          {
            "code": "415285009",
            "description": "Myelodysplastic syndrome with multilineage dysplasia",
            "attributes": null
          },
          {
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            "description": "Myelodysplastic syndrome with ring sideroblasts and multilineage dysplasia",
            "attributes": null
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          {
            "code": "415287001",
            "description": "Relapsing chronic myeloid leukemia",
            "attributes": null
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          {
            "code": "416180004",
            "description": "Hemoglobin SS disease without crisis",
            "attributes": null
          },
          {
            "code": "416214006",
            "description": "Sickle cell-hemoglobin D disease without crisis",
            "attributes": null
          },
          {
            "code": "416290001",
            "description": "Hemoglobin S sickling disorder without crisis",
            "attributes": null
          },
          {
            "code": "416484003",
            "description": "Sickle cell-hemoglobin E disease with crisis",
            "attributes": null
          },
          {
            "code": "416485002",
            "description": "Keratoconjunctivitis sicca due to graft-versus-host disease",
            "attributes": null
          },
          {
            "code": "416491000",
            "description": "Immune reconstitution inflammatory syndrome with uveitis",
            "attributes": null
          },
          {
            "code": "416638004",
            "description": "Sickle cell-hemoglobin E disease without crisis",
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            "description": "Sickling disorder due to hemoglobin S",
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            "code": "417683006",
            "description": "Sickle cell-hemoglobin C disease without crisis",
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            "description": "Sickle cell-hemoglobin D disease with crisis",
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            "description": "Neutropenia with dysgranulopoiesis",
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            "code": "420403001",
            "description": "Pneumocystosis with acquired immunodeficiency syndrome",
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            "description": "Malignant lymphoma of the eye region",
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            "code": "420544002",
            "description": "Bacterial pneumonia with acquired immunodeficiency syndrome",
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            "code": "420787001",
            "description": "Pneumococcal pneumonia with acquired immunodeficiency syndrome",
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            "description": "Intraocular non-Hodgkin malignant lymphoma",
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            "description": "T-lymphoblastic leukemia/lymphoblastic lymphoma",
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            "description": "Candidiasis of lung with acquired immunodeficiency syndrome",
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            "code": "421102007",
            "description": "Aplastic anemia with acquired immunodeficiency syndrome",
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            "code": "421246008",
            "description": "T-lymphoblastic lymphoma",
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            "description": "Primary lymphoma of brain with acquired immunodeficiency syndrome",
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            "description": "Agranulocytosis with acquired immunodeficiency syndrome",
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            "code": "421508002",
            "description": "Viral pneumonia with acquired immunodeficiency syndrome",
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            "code": "421671002",
            "description": "Pneumonia with acquired immunodeficiency syndrome",
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            "code": "422003001",
            "description": "Cachexia associated with acquired immunodeficiency syndrome",
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            "description": "Lymphoma of retroperitoneal space",
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            "code": "423032007",
            "description": "Leukemic infiltration of orbit",
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            "description": "Idiopathic hypereosinophilic syndrome",
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            "code": "423486005",
            "description": "Disseminated eosinophilic collagen disease",
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            "description": "Transplantation of ileum",
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            "code": "425657001",
            "description": "Osteosclerotic myeloma",
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            "code": "425688002",
            "description": "Philadelphia chromosome-positive acute lymphoblastic leukemia",
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            "description": "Subacute myeloid leukemia in remission",
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            "description": "Disorder of immune reconstitution",
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            "description": "Acute promyelocytic leukemia, FAB M3, in remission",
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            "description": "Precursor B-cell acute lymphoblastic leukemia in remission",
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            "code": "426071002",
            "description": "Hodgkin's disease in remission",
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            "code": "426124006",
            "description": "Acute myeloid leukemia with maturation, FAB M2, in remission",
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            "code": "426202004",
            "description": "Immune reconstitution inflammatory syndrome",
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            "code": "426217000",
            "description": "Aleukemic leukemia in remission",
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            "code": "426248008",
            "description": "Aleukemic lymphoid leukemia in remission",
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            "code": "426336007",
            "description": "Solitary osseous myeloma",
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            "code": "426370008",
            "description": "Subacute lymphoid leukemia in remission",
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            "code": "426425001",
            "description": "Transplant of bone marrow from sibling donor",
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            "code": "426463009",
            "description": "Allotransplantation of ileum",
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            "code": "426598005",
            "description": "Amyloid light-chain nephropathy",
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            "code": "426642002",
            "description": "Erythroleukemia, FAB M6 in remission",
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            "code": "426768001",
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            "description": "Hodgkin's disease, lymphocytic depletion of lymph nodes of head",
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            "description": "Subacute leukemia in remission",
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            "description": "Malignant lymphoma in remission",
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            "description": "Immunoproliferative neoplasm in remission",
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            "description": "Transplant of bone marrow from matched unrelated donor",
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            "code": "427642009",
            "description": "T-lymphoblastic leukemia in remission",
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            "description": "History of monocytic leukemia",
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            "description": "Disorder related to transplantation",
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            "description": "Disorder affecting transplanted structure",
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            "description": "Smoldering chronic lymphocytic leukemia",
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            "description": "Macrophage activation syndrome",
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            "description": "Basophilic leukemoid reaction",
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            "description": "Accelerated rejection of bone marrow transplant",
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            "code": "431505005",
            "description": "Rejection of intestine transplant",
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            "code": "431506006",
            "description": "Rejection of pancreas transplant",
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            "description": "Acute rejection of bone marrow transplant",
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            "description": "Chronic rejection of bone marrow transplant",
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            "code": "432782005",
            "description": "Hyperacute rejection of bone marrow transplant",
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            "code": "43355006",
            "description": "Eosinopenia",
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            "code": "433592008",
            "description": "Acute rejection of pancreas transplant",
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            "description": "Hyperacute rejection of intestine transplant",
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            "code": "433804007",
            "description": "Accelerated rejection of intestine transplant",
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            "code": "433809002",
            "description": "Accelerated rejection of pancreas transplant",
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            "code": "434202008",
            "description": "Hyperacute rejection of pancreas transplant",
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            "description": "Acute rejection of intestine transplant",
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            "description": "Chronic rejection of intestine transplant",
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            "description": "Chronic rejection of pancreas transplant",
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            "description": "Secondary aplastic anemia",
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            "description": "Hemoglobin SS disease with vasoocclusive crisis",
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            "description": "Asymptomatic multiple myeloma",
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            "description": "Indolent multiple myeloma",
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            "description": "History of sickle cell anemia",
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            "description": "Mantle cell lymphoma of spleen",
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            "description": "Large cell lymphoma of intrapelvic lymph nodes",
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            "description": "Calcification of spleen",
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            "code": "442459007",
            "description": "Combined immunodeficiency disease",
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            "code": "442537007",
            "description": "Non-Hodgkin lymphoma associated with Human immunodeficiency virus infection",
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            "description": "Transplant of bone marrow from unmatched unrelated donor",
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            "description": "T lymphocyte disorder",
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            "code": "4434006",
            "description": "Bloom syndrome",
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            "code": "443487006",
            "description": "Mantle cell lymphoma",
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            "description": "Acute sickle cell splenic sequestration crisis",
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            "description": "Graft versus host disease of skin",
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            "code": "444597005",
            "description": "Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue of stomach",
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            "description": "Primary mediastinal (thymic) large B-cell lymphoma",
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            "description": "Acute myeloid leukemia with t(9:11)(p22;q23); MLLT3-MLL",
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            "description": "Malignant blastic plasmacytoid dendritic cell neoplasm",
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            "description": "Juvenile myelomonocytic leukemia",
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            "description": "Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue",
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            "description": "Hepatosplenic T-cell lymphoma",
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            "description": "Acute myeloid leukemia with myelodysplasia-related changes",
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            "description": "Myelodysplastic/myeloproliferative disease",
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            "description": "Allogeneic bone marrow transplantation without purging",
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            "description": "Allogeneic bone marrow transplantation with purging",
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            "description": "Sarcoma of dendritic cells (accessory cells)",
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            "description": "Marginal zone lymphoma",
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            "description": "Myelodysplastic/myeloproliferative neoplasm, unclassifiable",
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            "description": "Lymphoma of pylorus of stomach",
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            "description": "Lymphoma of fundus of stomach",
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            "description": "Lymphoma of pyloric antrum of stomach",
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            "description": "Lymphoma of greater curvature of stomach",
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            "description": "Lymphoma of cardia of stomach",
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            "description": "Non-Hodgkin's lymphoma of extranodal site",
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            "description": "Anaplastic lymphoma kinase negative anaplastic large cell lymphoma",
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            "description": "Diffuse non-Hodgkin's lymphoma of prostate",
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            "description": "Follicular non-Hodgkin's lymphoma of prostate",
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            "description": "Non-Hodgkin's lymphoma of bone",
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            "description": "Follicular non-Hodgkin's lymphoma of nose",
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            "description": "Non-Hodgkin's lymphoma of central nervous system",
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            "description": "Lymphoma of lesser curvature of stomach",
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            "code": "448317000",
            "description": "Follicular non-Hodgkin's lymphoma of soft tissue",
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            "description": "Diffuse non-Hodgkin's lymphoma of nasopharynx",
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            "description": "Non-Hodgkin's lymphoma of intestine",
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            "code": "448371005",
            "description": "Non-Hodgkin's lymphoma of nasopharynx",
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            "description": "Non-Hodgkin's lymphoma of lung",
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            "description": "Non-Hodgkin's lymphoma of ovary",
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            "code": "448384001",
            "description": "Non-Hodgkin's lymphoma of nose",
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            "description": "Non-Hodgkin's lymphoma of oral cavity",
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            "description": "Non-Hodgkin's lymphoma of testis",
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            "description": "Non-Hodgkin's lymphoma of skin",
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            "description": "Diffuse non-Hodgkin's lymphoma of testis",
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            "description": "Diffuse non-Hodgkin's lymphoma of internal part of mouth",
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            "description": "Lymphoma of pelvis",
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            "description": "Lymphoma of body of stomach",
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            "description": "Diffuse non-Hodgkin's lymphoma of extranodal site",
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            "description": "Follicular non-Hodgkin's lymphoma of extranodal site",
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            "description": "Diffuse non-Hodgkin's lymphoma of uterine cervix",
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            "code": "448609001",
            "description": "Diffuse non-Hodgkin's lymphoma of ovary",
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            "code": "448663003",
            "description": "Diffuse non-Hodgkin's lymphoma of stomach",
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            "description": "Follicular non-Hodgkin's lymphoma of bone",
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            "description": "Follicular non-Hodgkin's lymphoma of lung",
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            "description": "Non-Hodgkin's lymphoma of stomach",
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            "description": "Non-Hodgkin's lymphoma of soft tissue",
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            "code": "448774004",
            "description": "Non-Hodgkin's lymphoma of uterine cervix",
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            "description": "Follicular non-Hodgkin's lymphoma of skin",
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            "description": "Diffuse non-Hodgkin's lymphoma of lung",
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            "description": "Follicular non-Hodgkin's lymphoma of central nervous system",
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            "description": "Lymphoma of lower esophagus",
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            "description": "Follicular non-Hodgkin's lymphoma of tonsil",
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            "description": "Follicular non-Hodgkin's lymphoma of uterine cervix",
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            "description": "Follicular non-Hodgkin's lymphoma of internal part of mouth",
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            "description": "Diffuse non-Hodgkin's lymphoma of nose",
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            "description": "Lymphoma of gastrointestinal tract",
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            "description": "Lymphoma of small intestine",
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            "description": "Lymphoma of cardioesophageal junction",
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            "description": "Philadelphia chromosome positive chronic myelogenous leukemia",
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            "code": "449173006",
            "description": "Diffuse non-Hodgkin's lymphoma of tonsil",
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            "description": "Diffuse non-Hodgkin's lymphoma of intestine",
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            "code": "449177007",
            "description": "Diffuse non-Hodgkin's lymphoma of bone",
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            "description": "Kappa light chain deficiency",
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            "code": "449216004",
            "description": "Diffuse non-Hodgkin's lymphoma of soft tissue",
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            "description": "Diffuse non-Hodgkin's lymphoma of skin",
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            "description": "Lymphoma of sigmoid colon",
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            "description": "Follicular non-Hodgkin's lymphoma of nasopharynx",
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            "description": "Diffuse follicle center lymphoma",
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            "description": "Diffuse non-Hodgkin's lymphoma of central nervous system",
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            "description": "Follicular non-Hodgkin's lymphoma of stomach",
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            "description": "Non-Hodgkin's lymphoma of tonsil",
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            "description": "Follicular non-Hodgkin's lymphoma of ovary",
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            "description": "Non-Hodgkin's lymphoma of prostate",
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            "description": "Lambda light chain deficiency",
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            "description": "Philadelphia chromosome negative chronic myelogenous leukemia",
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            "description": "Adenosine deaminase deficiency",
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            "code": "449418000",
            "description": "Follicular non-Hodgkin's lymphoma of testis",
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            "description": "Follicular non-Hodgkin's lymphoma of intestine",
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            "description": "Diffuse infiltrative lymphocytosis syndrome",
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            "description": "Interleukin-12 deficiency",
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            "description": "Celiac infantilism",
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            "description": "Severe combined immunodeficiency due to absent interleukin-2 production",
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            "description": "[X]Unspecified B-cell non-Hodgkin's lymphoma",
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            "description": "Kappa light chain disease",
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            "code": "46280001",
            "description": "Autologous bone marrow transplant with purging",
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            "code": "46359005",
            "description": "Neutropenia associated with infectious disease",
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            "code": "46760003",
            "description": "Estren-Dameshek anemia",
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            "code": "47024008",
            "description": "Sickle cell-hemoglobin E disease",
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            "code": "47144000",
            "description": "Acute neutrophilia",
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            "code": "473058009",
            "description": "History of lymphoid leukemia",
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            "code": "47318007",
            "description": "Drug-induced neutropenia",
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            "code": "47516005",
            "description": "Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin",
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            "code": "47650006",
            "description": "Graft versus host reaction",
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            "code": "48119005",
            "description": "Dysplasia of thymus gland with immunodeficiency",
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          {
            "code": "48794007",
            "description": "Human immunodeficiency virus infection with infectious mononucleosis-like syndrome",
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            "code": "48813009",
            "description": "Lymphocytopenia",
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          {
            "code": "49555001",
            "description": "Severe combined immunodeficiency due to absent T cell receptor",
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            "code": "50220002",
            "description": "Cellular immunologic aplastic anemia",
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            "code": "50926003",
            "description": "Job's syndrome",
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          {
            "code": "51319002",
            "description": "Light chain disease",
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          {
            "code": "51577008",
            "description": "Wilson-Mikity syndrome",
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            "code": "51615001",
            "description": "Fibrosis of lung",
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          {
            "code": "52064007",
            "description": "Biclonal gammopathy",
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            "code": "52079000",
            "description": "Congenital human immunodeficiency virus infection",
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            "code": "52967002",
            "description": "Myelofibrosis",
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          {
            "code": "54087003",
            "description": "Hairy cell leukemia",
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            "code": "54097007",
            "description": "White blood cell disorder",
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            "code": "55444004",
            "description": "Transient neonatal neutropenia",
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          {
            "code": "55602000",
            "description": "Nezelof's syndrome",
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            "code": "55907008",
            "description": "Acquired aplastic anemia",
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            "code": "56118002",
            "description": "Congenital syphilitic splenomegaly",
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          {
            "code": "56338005",
            "description": "Splenic fibrosis",
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          {
            "code": "56918001",
            "description": "Dose-related drug-induced neutropenia",
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          {
            "code": "58034007",
            "description": "Congenital hypergammaglobulinemia",
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          {
            "code": "58381000",
            "description": "Hypersplenism",
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          {
            "code": "58390007",
            "description": "Allogeneic bone marrow transplantation",
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          {
            "code": "58606001",
            "description": "Primary immune deficiency disorder",
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          {
            "code": "58639003",
            "description": "Doan-Wiseman syndrome",
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          {
            "code": "58648008",
            "description": "Benign monoclonal gammopathy",
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          {
            "code": "5876000",
            "description": "Acquired pancytopenia",
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          {
            "code": "58776007",
            "description": "Autologous bone marrow transplant",
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          {
            "code": "58961005",
            "description": "Lethal midline granuloma",
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          {
            "code": "60194009",
            "description": "Distal subtotal pancreatectomy with splenectomy",
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          {
            "code": "60620005",
            "description": "Epsilon heavy chain disease",
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          {
            "code": "606731000000100",
            "description": "Celiac disease NOS",
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            "code": "60743005",
            "description": "Purine-nucleoside phosphorylase deficiency",
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            "code": "61291000119103",
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            "code": "61301000119102",
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            "code": "61493004",
            "description": "Mu heavy chain disease",
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          {
            "code": "61535006",
            "description": "Transplantation of spleen",
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            "code": "61715008",
            "description": "Celiac disease with diffuse intestinal ulceration",
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            "code": "61777009",
            "description": "Thalassemia-hemoglobin C disease",
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            "code": "62438007",
            "description": "Transplantation of pancreas",
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            "code": "63484008",
            "description": "Drug-induced neutrophilia",
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            "code": "64249002",
            "description": "Allergic eosinophilia",
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            "code": "6471000179103",
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          {
            "code": "65399007",
            "description": "Langerhans cell histiocytosis",
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          {
            "code": "65623009",
            "description": "Immune neutropenia",
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          {
            "code": "65880007",
            "description": "X-linked agammaglobulinemia",
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          {
            "code": "66703008",
            "description": "Infection-associated hemophagocytic syndrome",
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          {
            "code": "66876008",
            "description": "Lambda light chain disease",
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          {
            "code": "67562009",
            "description": "Heterotransplant of pancreas",
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            "code": "676112841000119101",
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            "description": "History of mycosis fungoides",
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            "code": "68504005",
            "description": "Ataxia-telangiectasia syndrome",
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          {
            "code": "685061000119108",
            "description": "Hemoglobin C beta plus thalassemia",
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          {
            "code": "685071000119102",
            "description": "Hemoglobin C beta zero thalassemia",
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          {
            "code": "685081000119104",
            "description": "Hemoglobin D beta plus thalassemia",
            "attributes": null
          },
          {
            "code": "685091000119101",
            "description": "Hemoglobin D beta zero thalassemia",
            "attributes": null
          },
          {
            "code": "685101000119106",
            "description": "Hemoglobin E beta plus thalassemia",
            "attributes": null
          },
          {
            "code": "685111000119109",
            "description": "Hemoglobin E beta zero thalassemia",
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          {
            "code": "686961000119104",
            "description": "Mycosis fungoides of axillary lymph nodes",
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          {
            "code": "686981000119108",
            "description": "Mycosis fungoides of inguinal lymph node",
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          {
            "code": "686991000119106",
            "description": "Mycosis fungoides of lower limb lymph node",
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          {
            "code": "68712004",
            "description": "Lymphocytic hypoplasia",
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          {
            "code": "688271000119100",
            "description": "Sézary syndrome of inguinal lymph nodes",
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          {
            "code": "68979007",
            "description": "Heavy chain disease",
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          },
          {
            "code": "697919000",
            "description": "Pulmonary hypertension due to post-splenectomy hematological disorder",
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            "code": "698303004",
            "description": "Awaiting transplantation of bone marrow",
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            "code": "698362007",
            "description": "History of transplantation of pancreas",
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            "code": "698367001",
            "description": "History of transplantation of intestine",
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            "description": "Acute monoblastic leukemia in remission",
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            "description": "History of malignant hematologic neoplasm",
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            "code": "699537002",
            "description": "Erdheim-Chester disease",
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          {
            "code": "699657009",
            "description": "Hepatosplenic gamma-delta cell lymphoma",
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            "code": "699818003",
            "description": "T-cell large granular lymphocytic leukemia",
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            "description": "Familial granulomatous inflammatory arthritis, dermatitis and uveitis",
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            "code": "699869003",
            "description": "Interleukin-1 receptor-associated kinase 4 deficiency",
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            "description": "Overwhelming infection in asplenic patient",
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            "description": "Sepsis in asplenic subject",
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          {
            "code": "700052007",
            "description": "Post-splenectomy sepsis",
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          {
            "code": "700057001",
            "description": "Emberger syndrome",
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          {
            "code": "702444009",
            "description": "Autoimmune lymphoproliferative syndrome",
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            "description": "Core binding factor acute myeloid leukemia",
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            "description": "Aplasia of spleen",
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            "code": "702785000",
            "description": "Large cell anaplastic lymphoma T cell and null cell type",
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            "code": "702786004",
            "description": "Follicular non-Hodgkin's lymphoma diffuse follicle center sub-type grade 1",
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            "code": "702977001",
            "description": "Follicular non-Hodgkin's lymphoma diffuse follicle center cell sub-type grade 2",
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            "description": "Acute myeloid leukemia with normal karyotype",
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            "description": "Trichohepatoenteric syndrome",
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            "code": "703523004",
            "description": "Spondyloenchondrodysplasia with immune dysregulation",
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            "description": "Anhidrotic ectodermal dysplasia with immune deficiency",
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            "code": "703626001",
            "description": "Anaplastic large cell lymphoma T-cell and null-cell primary systemic type",
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            "description": "Asplenia",
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            "description": "Phagocytic immunodeficiency",
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            "description": "Periodontitis co-occurrent with Chédiak-Higashi syndrome",
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            "description": "Plasma cell hyperplasia of bone marrow",
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            "description": "Periodontitis co-occurrent with acquired neutropenia",
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            "description": "Periodontitis co-occurrent with leukocyte adhesion deficiency",
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            "description": "STING-associated vasculopathy with onset in infancy",
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            "description": "Activated PI3K-delta syndrome",
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          {
            "code": "713260006",
            "description": "Subacute adenoviral encephalitis co-occurrent with human immunodeficiency virus infection",
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          {
            "code": "713275003",
            "description": "Splenomegaly co-occurrent with human immunodeficiency virus infection",
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            "code": "713278001",
            "description": "Neuralgia co-occurrent with human immunodeficiency virus infection",
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          {
            "code": "713297001",
            "description": "Candidiasis of esophagus co-occurrent with human immunodeficiency virus infection",
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            "description": "Myocarditis co-occurrent with human immunodeficiency virus infection",
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          {
            "code": "713320007",
            "description": "Radiculitis co-occurrent with human immunodeficiency virus infection",
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          {
            "code": "713325002",
            "description": "Primary cerebral lymphoma co-occurrent with human immunodeficiency virus infection",
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            "description": "Anemia co-occurrent with human immunodeficiency virus infection",
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            "description": "Hemophagocytic syndrome with human immunodeficiency virus infection",
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            "description": "Disseminated infection caused by Strongyloides co-occurrent with human immunodeficiency virus infection",
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          {
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            "description": "Chronic infection caused by herpes simplex virus co-occurrent with human immunodeficiency virus infection",
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            "description": "Reticulosarcoma co-occurrent with human immunodeficiency virus infection",
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            "description": "Disorder of respiratory system co-occurrent with human immunodeficiency virus infection",
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            "description": "Progressive multifocal leukoencephalopathy co-occurrent with human immunodeficiency virus infection",
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            "description": "Presenile dementia co-occurrent with human immunodeficiency virus infection",
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            "description": "Polyneuropathy co-occurrent with human immunodeficiency virus infection",
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            "description": "Organic brain syndrome co-occurrent with human immunodeficiency virus infection",
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            "description": "Candidiasis of mouth co-occurrent with human immunodeficiency virus infection",
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            "description": "Disorder of spinal cord co-occurrent with human immunodeficiency virus infection",
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            "description": "Disorder of kidney co-occurrent with human immunodeficiency virus infection",
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            "description": "Gastrointestinal malabsorption syndrome co-occurrent with human immunodeficiency virus infection",
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            "description": "Neuritis co-occurrent with human immunodeficiency virus infection",
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            "description": "Lymphadenopathy co-occurrent with human immunodeficiency virus infection",
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            "description": "Aplastic anemia co-occurrent with human immunodeficiency virus infection",
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            "description": "Primary effusion lymphoma",
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            "description": "Cardiomyopathy co-occurrent with human immunodeficiency virus infection",
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            "description": "Recurrent bacterial pneumonia co-occurrent with human immunodeficiency virus infection",
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            "description": "Disorder of peripheral nervous system co-occurrent with human immunodeficiency virus infection",
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            "description": "Agranulocytosis co-occurrent with human immunodeficiency virus infection",
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            "description": "Visual impairment co-occurrent with human immunodeficiency virus infection",
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            "description": "Infective arthritis co-occurrent with human immunodeficiency virus infection",
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            "description": "Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection",
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            "description": "Demyelinating disease of central nervous system co-occurrent with human immunodeficiency virus infection",
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            "code": "713544008",
            "description": "Bacterial pneumonia co-occurrent with human immunodeficiency virus infection",
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            "description": "Infection caused by Nocardia co-occurrent with human immunodeficiency virus infection",
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            "code": "713546005",
            "description": "Isosporiasis co-occurrent with human immunodeficiency virus infection",
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            "description": "Infectious gastroenteritis co-occurrent with human immunodeficiency virus infection",
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            "description": "Disorder of central nervous system co-occurrent with human immunodeficiency virus infection",
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            "description": "Malignant neoplastic disease co-occurrent with human immunodeficiency virus infection",
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            "description": "Nephrotic syndrome co-occurrent with human immunodeficiency virus infection",
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            "description": "Renal failure syndrome co-occurrent with human immunodeficiency virus infection",
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            "description": "Diffuse non-Hodgkin immunoblastic lymphoma co-occurrent with human immunodeficiency virus infection",
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            "description": "Infection caused by Cytomegalovirus co-occurrent with human immunodeficiency virus infection",
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            "description": "Infection caused by Coccidia co-occurrent with human immunodeficiency virus infection",
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          {
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            "description": "Infection caused by herpes simplex virus co-occurrent with human immunodeficiency virus infection",
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            "description": "Pyrexia of unknown origin co-occurrent with human immunodeficiency virus infection",
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            "description": "Infection caused by Aspergillus co-occurrent with human immunodeficiency virus infection",
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            "description": "Infection caused by herpes zoster virus co-occurrent with human immunodeficiency virus infection",
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            "code": "713734009",
            "description": "Infection caused by Dermatophyte co-occurrent with human immunodeficiency virus infection",
            "attributes": null
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          {
            "code": "713844000",
            "description": "Dementia co-occurrent with human immunodeficiency virus infection",
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          {
            "code": "713845004",
            "description": "Infection caused by Cryptosporidium co-occurrent with human immunodeficiency virus infection",
            "attributes": null
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          {
            "code": "713880000",
            "description": "Opportunistic mycosis co-occurrent with human immunodeficiency virus infection",
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          {
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            "description": "Infection caused by Microsporidia co-occurrent with human immunodeficiency virus infection",
            "attributes": null
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          {
            "code": "713887002",
            "description": "Focal segmental glomerulosclerosis co-occurrent with human immunodeficiency virus infection",
            "attributes": null
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          {
            "code": "713897006",
            "description": "Burkitt lymphoma co-occurrent with human immunodeficiency virus infection",
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          {
            "code": "713964006",
            "description": "Multidermatomal infection caused by Herpes zoster co-occurrent with human immunodeficiency virus infection",
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            "description": "Disseminated atypical infection caused by Mycobacterium co-occurrent with human immunodeficiency virus infection",
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            "code": "714083007",
            "description": "Recurrent salmonella sepsis co-occurrent with human immunodeficiency virus infection",
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            "description": "Combined immunodeficiency due to calcium release activated calcium channel dysfunction",
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            "description": "Myeloid and lymphoid neoplasm with fibroblast growth factor receptor 1 abnormality",
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            "description": "Acute myeloid leukemia due to recurrent genetic abnormality",
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            "description": "Therapy related acute myeloid leukemia and myelodysplastic syndrome",
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            "description": "Acute leukemia of ambiguous lineage",
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            "description": "Aggressive natural killer-cell leukemia",
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            "description": "Follicular lymphoma of small intestine",
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            "description": "Adult T-cell leukemia/lymphoma of skin",
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            "description": "Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency",
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            "description": "Revesz syndrome",
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            "description": "B lymphoblastic leukemia lymphoma with t(9:22) (q34;q11.2); BCR-ABL 1",
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            "description": "T-cell histiocyte rich large B-cell lymphoma",
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            "description": "Plasmablastic lymphoma",
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            "description": "Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency",
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            "description": "Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency",
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            "description": "Autosomal recessive mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency",
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            "description": "Nodal marginal zone B-cell lymphoma",
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            "description": "Diffuse large B-cell lymphoma of central nervous system",
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            "description": "Human immunodeficiency virus World Health Organization 2007 stage 1 co-occurrent with malaria",
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            "description": "Human immunodeficiency virus World Health Organization 2007 stage 2 co-occurrent with tuberculosis",
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            "description": "Human immunodeficiency virus World Health Organization 2007 stage 2 co-occurrent with malaria",
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            "description": "Human immunodeficiency virus World Health Organization 2007 stage 3 co-occurrent with malaria",
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            "description": "Human immunodeficiency virus World Health Organization 2007 stage 4 co-occurrent with tuberculosis",
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            "description": "Human immunodeficiency virus World Health Organization 2007 stage 4 co-occurrent with malaria",
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            "description": "World Health Organization 2007 Human immunodeficiency virus infection clinical stage 1",
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            "description": "World Health Organization 2007 Human immunodeficiency virus infection clinical stage 2",
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            "description": "World Health Organization 2007 Human immunodeficiency virus infection clinical stage 3",
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            "description": "World Health Organization 2007 Human immunodeficiency virus infection clinical stage 4",
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            "description": "Therapy related acute myeloid leukemia due to and following administration of antineoplastic agent",
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            "description": "Chronic granulomatous disease, type IVA",
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            "description": "Acute myeloid leukemia with nucleophosmin 1 somatic mutation",
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            "description": "Severe combined immunodeficiency due to cytidine 5-prime triphosphate synthetase 1 deficiency",
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            "description": "Splenic marginal zone B-cell lymphoma",
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            "description": "Lichtenstein syndrome",
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            "description": "Idiopathic CD4 lymphocytopenia",
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            "description": "Hydroa vacciniforme-like lymphoma",
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            "description": "Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)",
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            "description": "Splenic diffuse red pulp small B-cell lymphoma",
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            "description": "Acute myeloid leukemia with CCAAT/enhancer binding protein alpha somatic mutation",
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            "description": "Isolated agammaglobulinemia",
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            "description": "Inherited acute myeloid leukemia",
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            "description": "Acute myeloid leukemia and myelodysplastic syndrome related to topoisomerase type 2 inhibitor",
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            "description": "Susceptibility to respiratory infection associated with CD8alpha chain mutation",
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            "description": "Ataxia pancytopenia syndrome",
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            "description": "Melanoma differentiation-associated gene 5 deficiency",
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            "description": "Human immunodeficiency virus (HIV) infection category B2",
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            "description": "Refractory celiac disease",
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            "description": "Combined immunodeficiency with faciooculoskeletal anomalies syndrome",
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            "code": "770942003",
            "description": "Kostmann syndrome",
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            "description": "Combined immunodeficiency due to serine/threonine kinase 4 deficiency",
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            "description": "Roifman syndrome",
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            "description": "Acquired hemophagocytic lymphohistiocytosis associated with malignant disease",
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            "description": "Recurrent Neisseria infection due to factor D deficiency",
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            "description": "Autosomal recessive severe congenital neutropenia due to glucose-6-phosphatase catalytic subunit 3 deficiency",
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            "description": "Noonan syndrome-like disorder with juvenile myelomonocytic leukemia",
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            "description": "Iatrogenic immunodeficiency-associated lymphoproliferative disorder",
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            "description": "Autosomal recessive severe congenital neutropenia due to jagunal homolog 1 deficiency",
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            "description": "Autosomal recessive severe congenital neutropenia due to C-X-C motif chemokine receptor 2 deficiency",
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            "description": "Autosomal recessive severe congenital neutropenia due to colony stimulating factor 3 receptor deficiency",
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            "description": "Non-chronic lymphocytic leukemia monoclonal B-cell lymphocytosis",
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            "description": "Hyperimmunoglobulin M syndrome with susceptibility to opportunistic infection",
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            "description": "Hereditary isolated aplastic anemia",
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            "description": "Adult-onset immunodeficiency with anti-interferon-gamma autoantibodies",
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            "description": "B-cell prolymphocytic leukemia in remission",
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            "description": "Juvenile myelomonocytic leukemia in remission",
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