[
  {
    "phenotype_id": "PH1710",
    "phenotype_version_id": 3635,
    "name": "Chronic paediatric conditions: Other endocrine (excluding diabetes)",
    "definition": "This code list is part of a set of harmonised code lists to identify chronic paediatric\nconditions across primary and secondary care datasets across the UK.\n\n- ICD-10 other endocrine conditions as per Hardelid 2014, mapped to SNOMED and Read v2 using CALIBER.\n- Excludes diabetes (see separate code list).\n- Includes e.g, hypothyroidism, hypopituitarism and adrenogenital disorders, congenital malformations of adrenal and other endocrine glands and disorders of calcium and phosphate metabolism.\n\n### Methods\n\nChronic paediatric conditions were defined as health problems requiring medical follow-up\nfor more than 12 months in 50% or more of cases. Code lists were produced by mapping\nexisting ICD-10 codes for chronic paediatric conditions to SNOMED and Read v2 codes\nusing the CALIBER R package, with review by paediatric sub-specialists.\n\nAn established ICD-10 code list of chronic paediatric conditions (Hardelid 2014)\nwas used as the basis for the new lists.[1]  Chronic paediatric conditions were defined\nas any health problem requiring medical follow-up (hospital admission, outpatient\nfollow up or use of support services such as physiotherapy) for more than 12 months\nin 50% or more of cases.[1]  A Chronic Paediatric Conditions Committee of paediatric\nsub-specialists was established. The original ICD-10 list was screened by two paediatricians\nand acute conditions removed, with disagreements resolved by a third paediatrician.\nConditions which were likely acute and would not fulfil our chronic disease definition\nwere excluded, including skeletal injuries and self-harm. Drug-induced conditions\nwere excluded as chronicity was not known. Infections other than human immunodeficiency\nvirus (HIV), hepatitis B or C, or congenital infections (syphilis / toxoplasmosis\n/ rubella / herpes simplex virus / cytomegalovirus) were excluded. Chronic sequelae\nof infections were retained.\n\nPublished code lists were then identified for Read v2 and SNOMED codes for well-characterised\nconditions including asthma, diabetes, cystic fibrosis and cancer. The remaining\nICD-10 codes were mapped to SNOMED and Read v2 codes using the CALIBER R package\nand Technology Reference Update Distribution NHS Data Migration tables [2] to produce\nnew code lists suitable for primary care data. These resulting code lists were screened\nby two sub-specialists to ensure conditions were chronic and in the correct subgroup\nwith disagreements resolved by a third clinician.\n\n### References:\n\n1. Hardelid P, Dattani N, Gilbert R. Estimating the prevalence of chronic conditions in children who die in England, Scotland and Wales: a data linkage cohort study. BMJ Open 2014; 4: e005331.\n2. CALIBER codelists-package: Generate ICD, Read and OPCS codelists in CALIBER codelists: Generate ICD10, Read and OPCS codelists, [https://rdrr.io/rforge/CALIBERcodelists/man/CALIBERcodelists-package.html](https://rdrr.io/rforge/CALIBERcodelists/man/CALIBERcodelists-package.html) (accessed 19 October 2022).\n\n",
    "implementation": "We have considered conditions to be active if they had been coded for in the preceding\nfive years. In addition, conditions from the following subgroups were considered\nto be permanent, therefore active if coded for at any time: metabolic, diabetes,\ncystic fibrosis, transplant, receiving palliative care, other congenital multisystem\nsyndromes and chromosomal abnormalities, immunological and cerebral palsy / paralysis\n(a subgroup of \"Other neurology\" code list).\n",
    "publications": [],
    "validation": "",
    "citation_requirements": "To our knowledge, these are the first set of harmonised code lists for chronic paediatric\nconditions that span commonly used primary and secondary care coding systems in the\nUK. We hope they will prove a valuable resource for the paediatric research community\nand welcome suggestions for further development ([Olivia.Swann@ed.ac.uk](mailto:Olivia.Swann@ed.ac.uk)).\n",
    "created": "2025-01-19T16:42:43.452979Z",
    "author": "Swann OV, Williams TC, Fraser LK, Farrell J, Parker M, Kennedy J, Seabourne M, Brophy S, Harrison EM, Docherty AB, Pollock L",
    "collections": [
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": null,
    "world_access": 2,
    "updated": "2025-01-19T16:42:43.438984Z",
    "sex": [
      {
        "name": "Both",
        "value": "3"
      }
    ],
    "type": [
      {
        "name": "Disease or syndrome",
        "value": "2"
      }
    ],
    "ontology": [
      {
        "name": "Paediatrics",
        "value": 842203
      },
      {
        "name": "Paediatric and Perinatal Pathology",
        "value": 842275
      }
    ],
    "phenoflowid": "",
    "data_sources": [
      {
        "name": "Hospital Episode Statistics Admitted Patient Care",
        "value": 2,
        "uid": "6599230a-df54-4615-937c-d724d239491f",
        "url": "https://healthdatagateway.org/en/dataset/875",
        "datasource_id": 875
      },
      {
        "name": "OpenSAFELY SNOMED CT",
        "value": 36,
        "datasource_id": 36
      },
      {
        "name": "Patient Episode Dataset for Wales (PEDW)",
        "value": 40,
        "uid": "4c33a5d2-164c-41d7-9797-dc2b008cc852",
        "url": "https://healthdatagateway.org/en/dataset/318",
        "datasource_id": 318
      },
      {
        "name": "Welsh Longitudinal General Practice Dataset (WLGP) - Welsh Primary Care",
        "value": 502,
        "uid": "33fc3ffd-aa4c-4a16-a32f-0c900aaea3d2",
        "url": "https://healthdatagateway.org/en/dataset/355",
        "datasource_id": 355
      }
    ],
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      },
      {
        "name": "ICD10 codes",
        "value": 4
      },
      {
        "name": "Read codes v2",
        "value": 5
      }
    ],
    "event_date_range": "2021/01/01 - 2021/01/01",
    "concept_information": [
      {
        "concept_id": 4164,
        "concept_version_id": 11524,
        "concept_name": "Other endocrine (excluding diabetes) (ICD-10)",
        "coding_system": {
          "id": 4,
          "name": "ICD10 codes",
          "description": "ICD10 Codes"
        },
        "phenotype_id": "PH1710",
        "phenotype_version_id": 3635,
        "phenotype_name": "Chronic paediatric conditions: Other endocrine (excluding diabetes)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "E00",
            "description": "Congenital iodine-deficiency syndrome",
            "attributes": null
          },
          {
            "code": "E000",
            "description": "Congenital iodine-deficiency syndrome, neurological type",
            "attributes": null
          },
          {
            "code": "E001",
            "description": "Congenital iodine-deficiency syndrome, myxoedematous type",
            "attributes": null
          },
          {
            "code": "E002",
            "description": "Congenital iodine-deficiency syndrome, mixed type",
            "attributes": null
          },
          {
            "code": "E009",
            "description": "Congenital iodine-deficiency syndrome, unspecified",
            "attributes": null
          },
          {
            "code": "E030",
            "description": "Congenital hypothyroidism with diffuse goitre",
            "attributes": null
          },
          {
            "code": "E031",
            "description": "Congenital hypothyroidism without goitre",
            "attributes": null
          },
          {
            "code": "E071",
            "description": "Dyshormogenetic goitre",
            "attributes": null
          },
          {
            "code": "E220",
            "description": "Acromegaly and pituitary gigantism",
            "attributes": null
          },
          {
            "code": "E230",
            "description": "Hypopituitarism",
            "attributes": null
          },
          {
            "code": "E244",
            "description": "Alcohol-induced pseudo-Cushing syndrome",
            "attributes": null
          },
          {
            "code": "E25",
            "description": "Adrenogenital disorders",
            "attributes": null
          },
          {
            "code": "E250",
            "description": "Congenital adrenogenital disorders associated with enzyme deficiency",
            "attributes": null
          },
          {
            "code": "E258",
            "description": "Other adrenogenital disorders",
            "attributes": null
          },
          {
            "code": "E259",
            "description": "Adrenogenital disorder, unspecified",
            "attributes": null
          },
          {
            "code": "E268",
            "description": "Other hyperaldosteronism",
            "attributes": null
          },
          {
            "code": "E271",
            "description": "Primary adrenocortical insufficiency",
            "attributes": null
          },
          {
            "code": "E272",
            "description": "Addisonian crisis",
            "attributes": null
          },
          {
            "code": "E274",
            "description": "Other and unspecified adrenocortical insufficiency",
            "attributes": null
          },
          {
            "code": "E291",
            "description": "Testicular hypofunction",
            "attributes": null
          },
          {
            "code": "E31",
            "description": "Polyglandular dysfunction",
            "attributes": null
          },
          {
            "code": "E310",
            "description": "Autoimmune polyglandular failure",
            "attributes": null
          },
          {
            "code": "E311",
            "description": "Polyglandular hyperfunction",
            "attributes": null
          },
          {
            "code": "E318",
            "description": "Other polyglandular dysfunction",
            "attributes": null
          },
          {
            "code": "E319",
            "description": "Polyglandular dysfunction, unspecified",
            "attributes": null
          },
          {
            "code": "E340",
            "description": "Carcinoid syndrome",
            "attributes": null
          },
          {
            "code": "E341",
            "description": "Other hypersecretion of intestinal hormones",
            "attributes": null
          },
          {
            "code": "E342",
            "description": "Ectopic hormone secretion, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "E345",
            "description": "Androgen resistance syndrome",
            "attributes": null
          },
          {
            "code": "E348",
            "description": "Other specified endocrine disorders",
            "attributes": null
          },
          {
            "code": "E350",
            "description": "Disorders of thyroid gland in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "E833",
            "description": "Disorders of phosphorus metabolism and phosphatases",
            "attributes": null
          },
          {
            "code": "E835",
            "description": "Disorders of calcium metabolism",
            "attributes": null
          },
          {
            "code": "Q891",
            "description": "Congenital malformations of adrenal gland",
            "attributes": null
          },
          {
            "code": "Q892",
            "description": "Congenital malformations of other endocrine glands",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4165,
        "concept_version_id": 11525,
        "concept_name": "Other endocrine (excluding diabetes) (Read v2)",
        "coding_system": {
          "id": 5,
          "name": "Read codes v2",
          "description": "Read codes v2"
        },
        "phenotype_id": "PH1710",
        "phenotype_version_id": 3635,
        "phenotype_name": "Chronic paediatric conditions: Other endocrine (excluding diabetes)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "A175.00",
            "description": "Tuberculosis of thyroid gland",
            "attributes": null
          },
          {
            "code": "C03..00",
            "description": "Congenital hypothyroidism",
            "attributes": null
          },
          {
            "code": "C030.00",
            "description": "Pendred's syndrome",
            "attributes": null
          },
          {
            "code": "C031.00",
            "description": "Goitrous cretin",
            "attributes": null
          },
          {
            "code": "C03..11",
            "description": "Cretinism",
            "attributes": null
          },
          {
            "code": "C03y.00",
            "description": "Other specified congenital hypothyroidism",
            "attributes": null
          },
          {
            "code": "C03y000",
            "description": "Congenital hypothyroidism with diffuse goitre",
            "attributes": null
          },
          {
            "code": "C03y100",
            "description": "Congenital hypothyroidism without goitre",
            "attributes": null
          },
          {
            "code": "C03z.00",
            "description": "Congenital hypothyroidism NOS",
            "attributes": null
          },
          {
            "code": "C03z.11",
            "description": "Congenital thyroid insufficiency",
            "attributes": null
          },
          {
            "code": "C03z.12",
            "description": "Cretinism",
            "attributes": null
          },
          {
            "code": "C061.00",
            "description": "Dyshormonogenic goitre",
            "attributes": null
          },
          {
            "code": "C0A..00",
            "description": "Congenital iodine deficiency syndrome",
            "attributes": null
          },
          {
            "code": "C0A0.00",
            "description": "Congenital iodine-deficiency syndrome, neurological type",
            "attributes": null
          },
          {
            "code": "C0A1.00",
            "description": "Congenital iodine-deficiency syndrome, myxoedematous type",
            "attributes": null
          },
          {
            "code": "C0A2.00",
            "description": "Congenital iodine-deficiency syndrome, mixed type",
            "attributes": null
          },
          {
            "code": "C10J.00",
            "description": "Insulin autoimmune syndrome",
            "attributes": null
          },
          {
            "code": "C10J000",
            "description": "Insulin autoimmune syndrome without complication",
            "attributes": null
          },
          {
            "code": "C130.00",
            "description": "Gigantism and acromegaly",
            "attributes": null
          },
          {
            "code": "C130100",
            "description": "Gigantism",
            "attributes": null
          },
          {
            "code": "C130.11",
            "description": "Growth hormone overproduction",
            "attributes": null
          },
          {
            "code": "C130200",
            "description": "Acromegaly",
            "attributes": null
          },
          {
            "code": "C130z00",
            "description": "Disorders of growth hormone excess NOS",
            "attributes": null
          },
          {
            "code": "C132.00",
            "description": "Panhypopituitarism",
            "attributes": null
          },
          {
            "code": "C132000",
            "description": "Idiopathic panhypopituitarism",
            "attributes": null
          },
          {
            "code": "C132.11",
            "description": "Hypopituitarism NOS",
            "attributes": null
          },
          {
            "code": "C132.12",
            "description": "Sheehan's syndrome",
            "attributes": null
          },
          {
            "code": "C132.13",
            "description": "Simmond's disease",
            "attributes": null
          },
          {
            "code": "C132200",
            "description": "Postinfarction panhypopituitarism",
            "attributes": null
          },
          {
            "code": "C132300",
            "description": "Postinfective panhypopituitarism",
            "attributes": null
          },
          {
            "code": "C132y00",
            "description": "Other specified panhypopituitarism",
            "attributes": null
          },
          {
            "code": "C132z00",
            "description": "Panhypopituitarism NOS",
            "attributes": null
          },
          {
            "code": "C133.00",
            "description": "Pituitary dwarfism",
            "attributes": null
          },
          {
            "code": "C133000",
            "description": "Isolated deficiency of growth hormone",
            "attributes": null
          },
          {
            "code": "C133.11",
            "description": "Lorain - Levi dwarfism",
            "attributes": null
          },
          {
            "code": "C133.12",
            "description": "Hypophyseal dwarfism",
            "attributes": null
          },
          {
            "code": "C133y00",
            "description": "Other specified pituitary dwarfism",
            "attributes": null
          },
          {
            "code": "C133y11",
            "description": "Ateliotic dwarf",
            "attributes": null
          },
          {
            "code": "C133z00",
            "description": "Pituitary dwarfism NOS",
            "attributes": null
          },
          {
            "code": "C134000",
            "description": "Prolactin deficiency",
            "attributes": null
          },
          {
            "code": "C134011",
            "description": "Hypoprolactinaemia",
            "attributes": null
          },
          {
            "code": "C134100",
            "description": "FSH - follicle stimulating hormone deficiency",
            "attributes": null
          },
          {
            "code": "C134200",
            "description": "LH - luteinising hormone deficiency",
            "attributes": null
          },
          {
            "code": "C134400",
            "description": "Isolated ACTH deficiency",
            "attributes": null
          },
          {
            "code": "C134411",
            "description": "ACTH deficiency",
            "attributes": null
          },
          {
            "code": "C134z11",
            "description": "Anterior pituitary hormone deficiency NEC",
            "attributes": null
          },
          {
            "code": "C139.00",
            "description": "Hypogonadotropic hypogonadism",
            "attributes": null
          },
          {
            "code": "C13A.00",
            "description": "Pituitary apoplexy",
            "attributes": null
          },
          {
            "code": "C150500",
            "description": "Alcohol-induced pseudo-Cushing's syndrome",
            "attributes": null
          },
          {
            "code": "C151.12",
            "description": "Bartter's syndrome",
            "attributes": null
          },
          {
            "code": "C151200",
            "description": "Bartter's syndrome",
            "attributes": null
          },
          {
            "code": "C152.00",
            "description": "Adrenogenital disorders",
            "attributes": null
          },
          {
            "code": "C152000",
            "description": "Congenital adrenogenital syndrome",
            "attributes": null
          },
          {
            "code": "C152100",
            "description": "Acquired adrenogenital syndrome",
            "attributes": null
          },
          {
            "code": "C152.11",
            "description": "Achard - Thiers syndrome",
            "attributes": null
          },
          {
            "code": "C152.12",
            "description": "Feminisation-adrenogenital",
            "attributes": null
          },
          {
            "code": "C152.13",
            "description": "Virilisation-adrenogenital",
            "attributes": null
          },
          {
            "code": "C152200",
            "description": "Defective synthesis of 21 hydroxylase",
            "attributes": null
          },
          {
            "code": "C152300",
            "description": "Defective synthesis of 11B hydroxylase",
            "attributes": null
          },
          {
            "code": "C152400",
            "description": "Defective synthesis of 3B hydroxysteroid dehydrogenase",
            "attributes": null
          },
          {
            "code": "C152500",
            "description": "Defective synthesis of 17-20 desmolase",
            "attributes": null
          },
          {
            "code": "C152600",
            "description": "Defective synthesis of 17 alpha hydroxylase",
            "attributes": null
          },
          {
            "code": "C152700",
            "description": "Other adrenogenital syndrome with salt loss",
            "attributes": null
          },
          {
            "code": "C152800",
            "description": "Other adrenogenital syndrome without mention of salt loss",
            "attributes": null
          },
          {
            "code": "C152811",
            "description": "Adrenogenital syndrome NOS",
            "attributes": null
          },
          {
            "code": "C152812",
            "description": "Congenital adrenal hyperplasia NEC",
            "attributes": null
          },
          {
            "code": "C152814",
            "description": "Pseudohermaphrodite, male with adrenocortical disorder",
            "attributes": null
          },
          {
            "code": "C152912",
            "description": "Precocious puberty with adrenal hyperplasia",
            "attributes": null
          },
          {
            "code": "C152A11",
            "description": "Virilisation - adrenogenital",
            "attributes": null
          },
          {
            "code": "C152A12",
            "description": "Pseudohermaphrodite,female with adrenocortical disorder",
            "attributes": null
          },
          {
            "code": "C152y00",
            "description": "Other specified adrenogenital disorder",
            "attributes": null
          },
          {
            "code": "C152z00",
            "description": "Adrenogenital disorder NOS",
            "attributes": null
          },
          {
            "code": "C154.00",
            "description": "Corticoadrenal insufficiency",
            "attributes": null
          },
          {
            "code": "C154000",
            "description": "Acute adrenal insufficiency",
            "attributes": null
          },
          {
            "code": "C154011",
            "description": "Addisonian crisis",
            "attributes": null
          },
          {
            "code": "C154012",
            "description": "Adrenal crisis",
            "attributes": null
          },
          {
            "code": "C154100",
            "description": "Addison's disease",
            "attributes": null
          },
          {
            "code": "C154300",
            "description": "Hypoaldosteronism",
            "attributes": null
          },
          {
            "code": "C154600",
            "description": "Addisonian crisis",
            "attributes": null
          },
          {
            "code": "C154700",
            "description": "Hyporeninaemic hypoaldosteronism",
            "attributes": null
          },
          {
            "code": "C154z00",
            "description": "Corticoadrenal insufficiency NOS",
            "attributes": null
          },
          {
            "code": "C154z11",
            "description": "Adrenal hypofunction",
            "attributes": null
          },
          {
            "code": "C154z12",
            "description": "Adrenal insufficiency NEC",
            "attributes": null
          },
          {
            "code": "C155.00",
            "description": "Other adrenal hypofunction",
            "attributes": null
          },
          {
            "code": "C155000",
            "description": "Adrenal medullary insufficiency",
            "attributes": null
          },
          {
            "code": "C155z00",
            "description": "Other adrenal hypofunction NOS",
            "attributes": null
          },
          {
            "code": "C164.11",
            "description": "Isosexual virilisation",
            "attributes": null
          },
          {
            "code": "C172000",
            "description": "Testicular hypofunction due to defect in adrenocortical hormone synthesis",
            "attributes": null
          },
          {
            "code": "C172011",
            "description": "Defective synthesis of 17B hydroxysteroid dehydrogenase",
            "attributes": null
          },
          {
            "code": "C172100",
            "description": "Eunuchism",
            "attributes": null
          },
          {
            "code": "C172.11",
            "description": "Eunuchoidism, hypogonadism",
            "attributes": null
          },
          {
            "code": "C172.12",
            "description": "Testicular hypogonadism",
            "attributes": null
          },
          {
            "code": "C17y000",
            "description": "Testicular feminization",
            "attributes": null
          },
          {
            "code": "C17y.11",
            "description": "Goldberg - Maxwell syndrome",
            "attributes": null
          },
          {
            "code": "C18..00",
            "description": "Polyglandular dysfunction and related disorders",
            "attributes": null
          },
          {
            "code": "C181.00",
            "description": "Other combinations of endocrine dysfunction",
            "attributes": null
          },
          {
            "code": "C181.11",
            "description": "Lloyd's syndrome",
            "attributes": null
          },
          {
            "code": "C181.12",
            "description": "Schmidt's syndrome",
            "attributes": null
          },
          {
            "code": "C182.00",
            "description": "Autoimmune polyglandular failure",
            "attributes": null
          },
          {
            "code": "C183.00",
            "description": "Polyglandular hyperfunction",
            "attributes": null
          },
          {
            "code": "C18y.00",
            "description": "Other specified polyglandular dysfunction",
            "attributes": null
          },
          {
            "code": "C18z.00",
            "description": "Polyglandular dysfunction NOS",
            "attributes": null
          },
          {
            "code": "C1z2.00",
            "description": "Carcinoid syndrome",
            "attributes": null
          },
          {
            "code": "C1z5.00",
            "description": "Androgen resistance syndrome",
            "attributes": null
          },
          {
            "code": "C1z5.11",
            "description": "Androgen insensitivity syndrome",
            "attributes": null
          },
          {
            "code": "C1zy000",
            "description": "Pineal gland dysfunction",
            "attributes": null
          },
          {
            "code": "C1zy100",
            "description": "Progeria",
            "attributes": null
          },
          {
            "code": "C1zy300",
            "description": "Leprechaunism",
            "attributes": null
          },
          {
            "code": "C1zy311",
            "description": "Donohue's syndrome",
            "attributes": null
          },
          {
            "code": "C1zy400",
            "description": "Werner's syndrome",
            "attributes": null
          },
          {
            "code": "C1zy500",
            "description": "Cyst of pineal gland",
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            "code": "C1zy600",
            "description": "Rabson-Mendenhall syndrome",
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          {
            "code": "C1zyz11",
            "description": "Werner's syndrome",
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          {
            "code": "C28A.00",
            "description": "Vitamin D-dependent rickets",
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            "code": "C28A000",
            "description": "Vitamin D-dependent rickets type I",
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            "code": "C28A100",
            "description": "Vitamin D-dependent rickets type II",
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            "code": "C353.00",
            "description": "Disorders of phosphorus metabolism",
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          },
          {
            "code": "C353000",
            "description": "Hypophosphatasia",
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          },
          {
            "code": "C353100",
            "description": "Hypophosphatasia rickets",
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          },
          {
            "code": "C353200",
            "description": "Vitamin-D-resistant rickets",
            "attributes": null
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          {
            "code": "C353211",
            "description": "Hypophosphataemic rickets",
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          {
            "code": "C353500",
            "description": "Acquired hypophosphataemia",
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            "code": "C353700",
            "description": "X-linked hypophosphataemic rickets",
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            "code": "C353800",
            "description": "Autosomal dominant hypophosphataemic rickets",
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            "code": "C353900",
            "description": "Autosomal recessive hypophosphataemic rickets",
            "attributes": null
          },
          {
            "code": "C353z00",
            "description": "Disorder of phosphorus metabolism NOS",
            "attributes": null
          },
          {
            "code": "C354.00",
            "description": "Disorders of calcium metabolism",
            "attributes": null
          },
          {
            "code": "C354200",
            "description": "Idiopathic hypercalcaemia",
            "attributes": null
          },
          {
            "code": "C354500",
            "description": "Hypercalcaemia familial benign",
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          {
            "code": "C354B00",
            "description": "Calciphylaxis",
            "attributes": null
          },
          {
            "code": "C354D00",
            "description": "Familial hypocalciuric hypercalcaemia",
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            "code": "C354y00",
            "description": "Other specified disorder of calcium metabolism",
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          },
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            "code": "C354z00",
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            "code": "C356.00",
            "description": "Disorders of phosphatases",
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            "description": "Liddle's syndrome",
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            "description": "[X]Other adrenogenital disorders",
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          },
          {
            "code": "Cyu4900",
            "description": "[X]Other and unspecified primary adrenocortical insufficiency",
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            "code": "Cyu4E00",
            "description": "[X]Other polyglandular dysfunction",
            "attributes": null
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            "code": "Cyu4G00",
            "description": "[X]Other hypersecretion of intestinal hormones",
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            "code": "F395000",
            "description": "Myopathy due to Addison's disease",
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            "code": "F395200",
            "description": "Myopathy due to hypopituitarism",
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            "description": "Pseudohypoaldosteronism",
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            "code": "K5B1000",
            "description": "Primary pituitary - hypothalamic infertility",
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          {
            "code": "K5B1100",
            "description": "Secondary pituitary - hypothalamic infertility",
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          {
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            "description": "Female infertility of pituitary - hypothalamic cause NOS",
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            "description": "Aberrant adrenal gland",
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            "description": "Absent adrenal gland",
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            "description": "Accessory adrenal gland",
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            "description": "Aplasia of adrenal gland",
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            "description": "Congenital cyst of adrenal gland",
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          },
          {
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          },
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          },
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          },
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            "description": "Congenital thyroid hypoplasia (disorder)",
            "attributes": null
          },
          {
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            "description": "Congenital atrophy of thyroid (disorder)",
            "attributes": null
          },
          {
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            "description": "Familial dyshormonogenetic goiter (disorder)",
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          },
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            "description": "Hypothyroidism due to iodide trapping defect (disorder)",
            "attributes": null
          },
          {
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            "description": "Hypothyroidism due to iodide organification defect (disorder)",
            "attributes": null
          },
          {
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            "description": "Thyroid hormone resistance syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "237560005",
            "description": "Generalized thyroid hormone resistance (disorder)",
            "attributes": null
          },
          {
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            "description": "Congenital iodine deficiency syndrome - mixed type (disorder)",
            "attributes": null
          },
          {
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            "description": "Congenital iodine deficiency syndrome - neurological type (disorder)",
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          },
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          },
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            "description": "Excessive cholecystokinin-pancreozymin secretion (disorder)",
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          },
          {
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            "description": "Abnormality of gastric inhibitory peptide secretion (disorder)",
            "attributes": null
          },
          {
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            "description": "Excessive gastric inhibitory peptide secretion (disorder)",
            "attributes": null
          },
          {
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            "attributes": null
          },
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            "description": "Abnormality of motilin secretion (disorder)",
            "attributes": null
          },
          {
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            "description": "Excessive motilin secretion (disorder)",
            "attributes": null
          },
          {
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            "attributes": null
          },
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            "description": "Excessive bombesin secretion (disorder)",
            "attributes": null
          },
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            "description": "Abnormality of serotonin secretion (disorder)",
            "attributes": null
          },
          {
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            "description": "Abnormality of neurotensine secretion (disorder)",
            "attributes": null
          },
          {
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            "description": "Anterior pituitary hyperplasia (disorder)",
            "attributes": null
          },
          {
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            "attributes": null
          },
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          },
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            "description": "Sheehan's syndrome (disorder)",
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          },
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          },
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          },
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            "description": "Idiopathic growth hormone deficiency (disorder)",
            "attributes": null
          },
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            "description": "Growth hormone neurosecretory dysfunction (disorder)",
            "attributes": null
          },
          {
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            "description": "Psychosocial growth hormone deficiency (disorder)",
            "attributes": null
          },
          {
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            "description": "Adrenocorticotropic hormone deficiency (disorder)",
            "attributes": null
          },
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            "description": "Idiopathic adrenocorticotropic hormone deficiency (disorder)",
            "attributes": null
          },
          {
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            "description": "Post-traumatic hypopituitarism (disorder)",
            "attributes": null
          },
          {
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            "description": "Hypopituitarism due to iron overload (disorder)",
            "attributes": null
          },
          {
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            "description": "Pituitary apoplexy (disorder)",
            "attributes": null
          },
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          },
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            "attributes": null
          },
          {
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            "description": "Glucocorticoid-suppressible hyperaldosteronism (disorder)",
            "attributes": null
          },
          {
            "code": "237747002",
            "description": "Feminization-adrenogenital syndrome (disorder)",
            "attributes": null
          },
          {
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            "description": "Pseudohermaphrodite, male with adrenocortical disorder (disorder)",
            "attributes": null
          },
          {
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            "description": "Virilization-adrenogenital syndrome (disorder)",
            "attributes": null
          },
          {
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            "description": "Pseudohermaphrodite, female with adrenocortical disorder (disorder)",
            "attributes": null
          },
          {
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            "description": "Congenital adrenal hyperplasia (disorder)",
            "attributes": null
          },
          {
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            "description": "Salt-losing congenital adrenal hyperplasia (disorder)",
            "attributes": null
          },
          {
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            "description": "Late onset congenital adrenal hyperplasia (disorder)",
            "attributes": null
          },
          {
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            "description": "Congenital adrenal hyperplasia - desmolase deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "237760008",
            "description": "Addison's disease with adrenoleucodystrophy (disorder)",
            "attributes": null
          },
          {
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            "description": "Adrenal insufficiency due to adrenal metastasis (disorder)",
            "attributes": null
          },
          {
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    "doi": "https://doi.org/10.48533/zydt-gb97",
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]