[
  {
    "phenotype_id": "PH3904",
    "phenotype_version_id": 9057,
    "name": "Asplenia or Dysfunction of the Spleen codes",
    "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 `SPLN_COV_COD` field in SARS\\-CoV2 COVID19 Vaccination Uptake Reporting Codes 20_21 v1, published by PRIMIS.\n\n\n© PRIMIS \\- the University of Nottingham 2021\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": "2026-01-26T23:38:43.803012Z",
    "author": "PRIMIS Covid Vaccination Uptake Reporting (old)",
    "collections": [
      {
        "name": "OpenCodelist",
        "value": 31
      },
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": {
      "id": 1,
      "slug": "opensafely",
      "name": "OpenSAFELY"
    },
    "world_access": 1,
    "updated": "2026-01-26T23:38:43.796136Z",
    "references": [],
    "signed_off": [],
    "methodology": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "primis-covid19-vacc-uptake-old/spln_cov_cod",
    "source_reference": "https://www.opencodelists.org/codelist/primis-covid19-vacc-uptake-old/spln_cov_cod/v1",
    "concept_information": [
      {
        "concept_id": 9234,
        "concept_version_id": 16719,
        "concept_name": "primis-covid19-vacc-uptake-old/spln_cov_cod/v1",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH3904",
        "phenotype_version_id": 9057,
        "phenotype_name": "Asplenia or Dysfunction of the Spleen codes",
        "code_attribute_header": [],
        "codes": [
          {
            "code": "10759351000119103",
            "description": "Sickle cell anemia in mother complicating childbirth",
            "attributes": null
          },
          {
            "code": "111572002",
            "description": "beta^0^ Thalassemia, nondeletion type",
            "attributes": null
          },
          {
            "code": "123617004",
            "description": "Fleckmilz",
            "attributes": null
          },
          {
            "code": "1239371000000103",
            "description": "Haemoglobin E beta zero thalassaemia",
            "attributes": null
          },
          {
            "code": "1239381000000101",
            "description": "Haemoglobin E beta plus thalassaemia",
            "attributes": null
          },
          {
            "code": "127040003",
            "description": "Sickle cell-hemoglobin SS disease",
            "attributes": null
          },
          {
            "code": "127041004",
            "description": "Sickle cell-beta-thalassemia",
            "attributes": null
          },
          {
            "code": "127042006",
            "description": "Sickle cell beta plus thalassemia",
            "attributes": null
          },
          {
            "code": "127043001",
            "description": "Sickle cell-beta^0^-thalassemia",
            "attributes": null
          },
          {
            "code": "127044007",
            "description": "Sickle cell-delta beta^0^-thalassemia",
            "attributes": null
          },
          {
            "code": "127045008",
            "description": "Sickle cell anemia with coexistent alpha-thalassemia",
            "attributes": null
          },
          {
            "code": "127047000",
            "description": "Sickle cell-hemoglobin Lepore disease",
            "attributes": null
          },
          {
            "code": "127048005",
            "description": "Sickle cell-Hemoglobin O Arab disease",
            "attributes": null
          },
          {
            "code": "161626009",
            "description": "History of splenectomy",
            "attributes": null
          },
          {
            "code": "1671000",
            "description": "Sago spleen",
            "attributes": null
          },
          {
            "code": "174776001",
            "description": "Total splenectomy",
            "attributes": null
          },
          {
            "code": "174778000",
            "description": "Total splenectomy and reimplantation of fragments",
            "attributes": null
          },
          {
            "code": "174789007",
            "description": "Embolization of spleen",
            "attributes": null
          },
          {
            "code": "17604001",
            "description": "Bilateral right-sidedness sequence",
            "attributes": null
          },
          {
            "code": "195340002",
            "description": "Embolism and thrombosis of the splenic artery",
            "attributes": null
          },
          {
            "code": "205735005",
            "description": "Hypoplasia of spleen",
            "attributes": null
          },
          {
            "code": "22996003",
            "description": "Splenic infarction",
            "attributes": null
          },
          {
            "code": "23269001",
            "description": "Double heterozygous sickling disorder",
            "attributes": null
          },
          {
            "code": "234319005",
            "description": "Splenectomy",
            "attributes": null
          },
          {
            "code": "234391009",
            "description": "Sickle cell anemia with high hemoglobin F",
            "attributes": null
          },
          {
            "code": "234392002",
            "description": "Hemoglobin E/beta thalassemia disease",
            "attributes": null
          },
          {
            "code": "234510005",
            "description": "Amyloidosis of spleen",
            "attributes": null
          },
          {
            "code": "236854007",
            "description": "Septic splenitis",
            "attributes": null
          },
          {
            "code": "23761004",
            "description": "Hyposplenism",
            "attributes": null
          },
          {
            "code": "25472008",
            "description": "Sickle cell-hemoglobin D disease",
            "attributes": null
          },
          {
            "code": "262821002",
            "description": "Avulsion of spleen",
            "attributes": null
          },
          {
            "code": "26682008",
            "description": "Homozygous beta thalassemia",
            "attributes": null
          },
          {
            "code": "27080008",
            "description": "beta^0^ Thalassemia, deletion type",
            "attributes": null
          },
          {
            "code": "275403002",
            "description": "Villous atrophy",
            "attributes": null
          },
          {
            "code": "275404008",
            "description": "Celiac rickets",
            "attributes": null
          },
          {
            "code": "275405009",
            "description": "Partial villous atrophy",
            "attributes": null
          },
          {
            "code": "300564004",
            "description": "Spleen absent",
            "attributes": null
          },
          {
            "code": "302961007",
            "description": "Hereditary splenic hypoplasia",
            "attributes": null
          },
          {
            "code": "314118002",
            "description": "Laparoscopic total splenectomy",
            "attributes": null
          },
          {
            "code": "33479006",
            "description": "Distal subtotal pancreatectomy with splenectomy and pancreaticojejunostomy",
            "attributes": null
          },
          {
            "code": "35434009",
            "description": "Sickle cell-hemoglobin C disease",
            "attributes": null
          },
          {
            "code": "36472007",
            "description": "Sickle cell-thalassemia disease",
            "attributes": null
          },
          {
            "code": "38096003",
            "description": "Functional asplenia",
            "attributes": null
          },
          {
            "code": "38970002",
            "description": "Doan-Wright syndrome",
            "attributes": null
          },
          {
            "code": "396330006",
            "description": "Celiac crisis",
            "attributes": null
          },
          {
            "code": "396331005",
            "description": "Celiac disease",
            "attributes": null
          },
          {
            "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": "416638004",
            "description": "Sickle cell-hemoglobin E disease without crisis",
            "attributes": null
          },
          {
            "code": "416826005",
            "description": "Sickle cell-thalassemia disease with crisis",
            "attributes": null
          },
          {
            "code": "417048006",
            "description": "Sickle cell-thalassemia disease without crisis",
            "attributes": null
          },
          {
            "code": "417279003",
            "description": "Hemoglobin S sickling disorder with crisis",
            "attributes": null
          },
          {
            "code": "417357006",
            "description": "Sickling disorder due to hemoglobin S",
            "attributes": null
          },
          {
            "code": "417425009",
            "description": "Hemoglobin SS disease with crisis",
            "attributes": null
          },
          {
            "code": "417517009",
            "description": "Sickle cell-hemoglobin C disease with crisis",
            "attributes": null
          },
          {
            "code": "417683006",
            "description": "Sickle cell-hemoglobin C disease without crisis",
            "attributes": null
          },
          {
            "code": "417748003",
            "description": "Sickle cell-hemoglobin D disease with crisis",
            "attributes": null
          },
          {
            "code": "440206000",
            "description": "Hemoglobin SS disease with vasoocclusive crisis",
            "attributes": null
          },
          {
            "code": "444108000",
            "description": "Acute sickle cell splenic sequestration crisis",
            "attributes": null
          },
          {
            "code": "47024008",
            "description": "Sickle cell-hemoglobin E disease",
            "attributes": null
          },
          {
            "code": "54006005",
            "description": "Hereditary persistence of fetal hemoglobin delta beta plus thalassemia",
            "attributes": null
          },
          {
            "code": "56338005",
            "description": "Splenic fibrosis",
            "attributes": null
          },
          {
            "code": "58381000",
            "description": "Hypersplenism",
            "attributes": null
          },
          {
            "code": "60194009",
            "description": "Distal subtotal pancreatectomy with splenectomy",
            "attributes": null
          },
          {
            "code": "61535006",
            "description": "Transplantation of spleen",
            "attributes": null
          },
          {
            "code": "61715008",
            "description": "Celiac disease with diffuse intestinal ulceration",
            "attributes": null
          },
          {
            "code": "700050004",
            "description": "Overwhelming infection in asplenic patient",
            "attributes": null
          },
          {
            "code": "700051000",
            "description": "Sepsis in asplenic subject",
            "attributes": null
          },
          {
            "code": "700052007",
            "description": "Post-splenectomy sepsis",
            "attributes": null
          },
          {
            "code": "702624008",
            "description": "Aplasia of spleen",
            "attributes": null
          },
          {
            "code": "707147002",
            "description": "Asplenia",
            "attributes": null
          },
          {
            "code": "711407000",
            "description": "Thrombocytopathy, asplenia and miosis",
            "attributes": null
          },
          {
            "code": "717156002",
            "description": "Biliary atresia with splenic malformation syndrome",
            "attributes": null
          },
          {
            "code": "722386009",
            "description": "Celiac disease with epilepsy and cerebral calcification syndrome",
            "attributes": null
          },
          {
            "code": "724639003",
            "description": "Asplenia following surgical procedure",
            "attributes": null
          },
          {
            "code": "726708009",
            "description": "Familial isolated congenital asplenia",
            "attributes": null
          },
          {
            "code": "73190000",
            "description": "epsilon gamma delta beta^0^ Thalassemia",
            "attributes": null
          },
          {
            "code": "75451007",
            "description": "Thalassemia major",
            "attributes": null
          },
          {
            "code": "76336008",
            "description": "Delta beta zero thalassemia",
            "attributes": null
          },
          {
            "code": "770593004",
            "description": "Refractory celiac disease",
            "attributes": null
          },
          {
            "code": "783254003",
            "description": "Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome",
            "attributes": null
          },
          {
            "code": "82893001",
            "description": "Splenic atrophy",
            "attributes": null
          },
          {
            "code": "861371000000102",
            "description": "Acquired absence of spleen",
            "attributes": null
          },
          {
            "code": "86715000",
            "description": "Beta zero thalassemia",
            "attributes": null
          },
          {
            "code": "89810003",
            "description": "^A^gamma delta beta^0^ thalassemia",
            "attributes": null
          },
          {
            "code": "91867008",
            "description": "Adult form of celiac disease",
            "attributes": null
          },
          {
            "code": "93030006",
            "description": "Congenital absence of spleen",
            "attributes": null
          },
          {
            "code": "93292008",
            "description": "Congenital hypoplasia of spleen",
            "attributes": null
          },
          {
            "code": "95846001",
            "description": "Red blood cell sequestration in spleen",
            "attributes": null
          }
        ]
      }
    ],
    "coding_system_release": "",
    "open_codelist_version_id": "2e33fba2",
    "open_codelist_version_tag": "v1",
    "status": 1,
    "doi": "https://doi.org/10.48533/rct4-ve88",
    "is_deleted": false,
    "publish_status": 2,
    "owner": "ieuan.scanlon",
    "template": {
      "id": 3,
      "name": "OpenCodelists Phenotype",
      "description": "OpenSafely's OpenCodelist Phenotype, visit https://www.opencodelists.org/ to learn more",
      "version_id": 1
    },
    "versions": [
      {
        "version_id": 9057,
        "version_name": "Asplenia or Dysfunction of the Spleen codes",
        "version_date": "2026-01-26T23:38:43.811850Z",
        "is_published": true,
        "is_latest": true
      }
    ]
  }
]