{
  "concept_id": 4165,
  "concept_version_id": 11525,
  "coding_system": {
    "id": 5,
    "name": "Read codes v2",
    "description": "Read codes v2"
  },
  "name": "Other endocrine (excluding diabetes) (Read v2)",
  "description": null,
  "author": "",
  "entry_date": "2025-01-19",
  "validation_performed": false,
  "validation_description": null,
  "publication_doi": "",
  "publication_link": "",
  "secondary_publication_links": null,
  "paper_published": false,
  "source_reference": "",
  "citation_requirements": null,
  "owner_access": 3,
  "group_access": 1,
  "world_access": 1,
  "tags": null,
  "collections": null,
  "created_by": null,
  "modified_by": null,
  "owner": null,
  "group": null,
  "phenotype_owner": "PH1710",
  "phenotype_owner_history_id": 3635,
  "requested_entity_id": null,
  "components": [
    {
      "id": 9992,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "text/csv",
      "codes": [
        {
          "id": 537207,
          "code": "A175.00",
          "description": "Tuberculosis of thyroid gland"
        },
        {
          "id": 537208,
          "code": "C03..00",
          "description": "Congenital hypothyroidism"
        },
        {
          "id": 537209,
          "code": "C03..11",
          "description": "Cretinism"
        },
        {
          "id": 537210,
          "code": "C030.00",
          "description": "Pendred's syndrome"
        },
        {
          "id": 537211,
          "code": "C031.00",
          "description": "Goitrous cretin"
        },
        {
          "id": 537212,
          "code": "C03y.00",
          "description": "Other specified congenital hypothyroidism"
        },
        {
          "id": 537213,
          "code": "C03y000",
          "description": "Congenital hypothyroidism with diffuse goitre"
        },
        {
          "id": 537214,
          "code": "C03y100",
          "description": "Congenital hypothyroidism without goitre"
        },
        {
          "id": 537215,
          "code": "C03z.00",
          "description": "Congenital hypothyroidism NOS"
        },
        {
          "id": 537216,
          "code": "C03z.11",
          "description": "Congenital thyroid insufficiency"
        },
        {
          "id": 537217,
          "code": "C03z.12",
          "description": "Cretinism"
        },
        {
          "id": 537218,
          "code": "C061.00",
          "description": "Dyshormonogenic goitre"
        },
        {
          "id": 537219,
          "code": "C0A..00",
          "description": "Congenital iodine deficiency syndrome"
        },
        {
          "id": 537220,
          "code": "C0A0.00",
          "description": "Congenital iodine-deficiency syndrome, neurological type"
        },
        {
          "id": 537221,
          "code": "C0A1.00",
          "description": "Congenital iodine-deficiency syndrome, myxoedematous type"
        },
        {
          "id": 537222,
          "code": "C0A2.00",
          "description": "Congenital iodine-deficiency syndrome, mixed type"
        },
        {
          "id": 537223,
          "code": "C10J.00",
          "description": "Insulin autoimmune syndrome"
        },
        {
          "id": 537224,
          "code": "C10J000",
          "description": "Insulin autoimmune syndrome without complication"
        },
        {
          "id": 537225,
          "code": "C130.00",
          "description": "Gigantism and acromegaly"
        },
        {
          "id": 537226,
          "code": "C130.11",
          "description": "Growth hormone overproduction"
        },
        {
          "id": 537227,
          "code": "C130100",
          "description": "Gigantism"
        },
        {
          "id": 537228,
          "code": "C130200",
          "description": "Acromegaly"
        },
        {
          "id": 537229,
          "code": "C130z00",
          "description": "Disorders of growth hormone excess NOS"
        },
        {
          "id": 537230,
          "code": "C132.00",
          "description": "Panhypopituitarism"
        },
        {
          "id": 537231,
          "code": "C132.11",
          "description": "Hypopituitarism NOS"
        },
        {
          "id": 537232,
          "code": "C132.12",
          "description": "Sheehan's syndrome"
        },
        {
          "id": 537233,
          "code": "C132.13",
          "description": "Simmond's disease"
        },
        {
          "id": 537234,
          "code": "C132000",
          "description": "Idiopathic panhypopituitarism"
        },
        {
          "id": 537235,
          "code": "C132200",
          "description": "Postinfarction panhypopituitarism"
        },
        {
          "id": 537236,
          "code": "C132300",
          "description": "Postinfective panhypopituitarism"
        },
        {
          "id": 537237,
          "code": "C132y00",
          "description": "Other specified panhypopituitarism"
        },
        {
          "id": 537238,
          "code": "C132z00",
          "description": "Panhypopituitarism NOS"
        },
        {
          "id": 537239,
          "code": "C133.00",
          "description": "Pituitary dwarfism"
        },
        {
          "id": 537240,
          "code": "C133.11",
          "description": "Lorain - Levi dwarfism"
        },
        {
          "id": 537241,
          "code": "C133.12",
          "description": "Hypophyseal dwarfism"
        },
        {
          "id": 537242,
          "code": "C133000",
          "description": "Isolated deficiency of growth hormone"
        },
        {
          "id": 537243,
          "code": "C133y00",
          "description": "Other specified pituitary dwarfism"
        },
        {
          "id": 537244,
          "code": "C133y11",
          "description": "Ateliotic dwarf"
        },
        {
          "id": 537245,
          "code": "C133z00",
          "description": "Pituitary dwarfism NOS"
        },
        {
          "id": 537246,
          "code": "C134000",
          "description": "Prolactin deficiency"
        },
        {
          "id": 537247,
          "code": "C134011",
          "description": "Hypoprolactinaemia"
        },
        {
          "id": 537248,
          "code": "C134100",
          "description": "FSH - follicle stimulating hormone deficiency"
        },
        {
          "id": 537249,
          "code": "C134200",
          "description": "LH - luteinising hormone deficiency"
        },
        {
          "id": 537250,
          "code": "C134400",
          "description": "Isolated ACTH deficiency"
        },
        {
          "id": 537251,
          "code": "C134411",
          "description": "ACTH deficiency"
        },
        {
          "id": 537252,
          "code": "C134z11",
          "description": "Anterior pituitary hormone deficiency NEC"
        },
        {
          "id": 537253,
          "code": "C139.00",
          "description": "Hypogonadotropic hypogonadism"
        },
        {
          "id": 537254,
          "code": "C13A.00",
          "description": "Pituitary apoplexy"
        },
        {
          "id": 537255,
          "code": "C150500",
          "description": "Alcohol-induced pseudo-Cushing's syndrome"
        },
        {
          "id": 537256,
          "code": "C151.12",
          "description": "Bartter's syndrome"
        },
        {
          "id": 537257,
          "code": "C151200",
          "description": "Bartter's syndrome"
        },
        {
          "id": 537258,
          "code": "C152.00",
          "description": "Adrenogenital disorders"
        },
        {
          "id": 537259,
          "code": "C152.11",
          "description": "Achard - Thiers syndrome"
        },
        {
          "id": 537260,
          "code": "C152.12",
          "description": "Feminisation-adrenogenital"
        },
        {
          "id": 537261,
          "code": "C152.13",
          "description": "Virilisation-adrenogenital"
        },
        {
          "id": 537262,
          "code": "C152000",
          "description": "Congenital adrenogenital syndrome"
        },
        {
          "id": 537263,
          "code": "C152100",
          "description": "Acquired adrenogenital syndrome"
        },
        {
          "id": 537264,
          "code": "C152200",
          "description": "Defective synthesis of 21 hydroxylase"
        },
        {
          "id": 537265,
          "code": "C152300",
          "description": "Defective synthesis of 11B hydroxylase"
        },
        {
          "id": 537266,
          "code": "C152400",
          "description": "Defective synthesis of 3B hydroxysteroid dehydrogenase"
        },
        {
          "id": 537267,
          "code": "C152500",
          "description": "Defective synthesis of 17-20 desmolase"
        },
        {
          "id": 537268,
          "code": "C152600",
          "description": "Defective synthesis of 17 alpha hydroxylase"
        },
        {
          "id": 537269,
          "code": "C152700",
          "description": "Other adrenogenital syndrome with salt loss"
        },
        {
          "id": 537270,
          "code": "C152800",
          "description": "Other adrenogenital syndrome without mention of salt loss"
        },
        {
          "id": 537271,
          "code": "C152811",
          "description": "Adrenogenital syndrome NOS"
        },
        {
          "id": 537272,
          "code": "C152812",
          "description": "Congenital adrenal hyperplasia NEC"
        },
        {
          "id": 537273,
          "code": "C152814",
          "description": "Pseudohermaphrodite, male with adrenocortical disorder"
        },
        {
          "id": 537274,
          "code": "C152912",
          "description": "Precocious puberty with adrenal hyperplasia"
        },
        {
          "id": 537275,
          "code": "C152A11",
          "description": "Virilisation - adrenogenital"
        },
        {
          "id": 537276,
          "code": "C152A12",
          "description": "Pseudohermaphrodite,female with adrenocortical disorder"
        },
        {
          "id": 537277,
          "code": "C152y00",
          "description": "Other specified adrenogenital disorder"
        },
        {
          "id": 537278,
          "code": "C152z00",
          "description": "Adrenogenital disorder NOS"
        },
        {
          "id": 537279,
          "code": "C154.00",
          "description": "Corticoadrenal insufficiency"
        },
        {
          "id": 537280,
          "code": "C154000",
          "description": "Acute adrenal insufficiency"
        },
        {
          "id": 537281,
          "code": "C154011",
          "description": "Addisonian crisis"
        },
        {
          "id": 537282,
          "code": "C154012",
          "description": "Adrenal crisis"
        },
        {
          "id": 537283,
          "code": "C154100",
          "description": "Addison's disease"
        },
        {
          "id": 537284,
          "code": "C154300",
          "description": "Hypoaldosteronism"
        },
        {
          "id": 537285,
          "code": "C154600",
          "description": "Addisonian crisis"
        },
        {
          "id": 537286,
          "code": "C154700",
          "description": "Hyporeninaemic hypoaldosteronism"
        },
        {
          "id": 537287,
          "code": "C154z00",
          "description": "Corticoadrenal insufficiency NOS"
        },
        {
          "id": 537288,
          "code": "C154z11",
          "description": "Adrenal hypofunction"
        },
        {
          "id": 537289,
          "code": "C154z12",
          "description": "Adrenal insufficiency NEC"
        },
        {
          "id": 537290,
          "code": "C155.00",
          "description": "Other adrenal hypofunction"
        },
        {
          "id": 537291,
          "code": "C155000",
          "description": "Adrenal medullary insufficiency"
        },
        {
          "id": 537292,
          "code": "C155z00",
          "description": "Other adrenal hypofunction NOS"
        },
        {
          "id": 537293,
          "code": "C164.11",
          "description": "Isosexual virilisation"
        },
        {
          "id": 537294,
          "code": "C172.11",
          "description": "Eunuchoidism, hypogonadism"
        },
        {
          "id": 537295,
          "code": "C172.12",
          "description": "Testicular hypogonadism"
        },
        {
          "id": 537296,
          "code": "C172000",
          "description": "Testicular hypofunction due to defect in adrenocortical hormone synthesis"
        },
        {
          "id": 537297,
          "code": "C172011",
          "description": "Defective synthesis of 17B hydroxysteroid dehydrogenase"
        },
        {
          "id": 537298,
          "code": "C172100",
          "description": "Eunuchism"
        },
        {
          "id": 537299,
          "code": "C17y.11",
          "description": "Goldberg - Maxwell syndrome"
        },
        {
          "id": 537300,
          "code": "C17y000",
          "description": "Testicular feminization"
        },
        {
          "id": 537301,
          "code": "C18..00",
          "description": "Polyglandular dysfunction and related disorders"
        },
        {
          "id": 537302,
          "code": "C181.00",
          "description": "Other combinations of endocrine dysfunction"
        },
        {
          "id": 537303,
          "code": "C181.11",
          "description": "Lloyd's syndrome"
        },
        {
          "id": 537304,
          "code": "C181.12",
          "description": "Schmidt's syndrome"
        },
        {
          "id": 537305,
          "code": "C182.00",
          "description": "Autoimmune polyglandular failure"
        },
        {
          "id": 537306,
          "code": "C183.00",
          "description": "Polyglandular hyperfunction"
        },
        {
          "id": 537307,
          "code": "C18y.00",
          "description": "Other specified polyglandular dysfunction"
        },
        {
          "id": 537308,
          "code": "C18z.00",
          "description": "Polyglandular dysfunction NOS"
        },
        {
          "id": 537309,
          "code": "C1z2.00",
          "description": "Carcinoid syndrome"
        },
        {
          "id": 537310,
          "code": "C1z5.00",
          "description": "Androgen resistance syndrome"
        },
        {
          "id": 537311,
          "code": "C1z5.11",
          "description": "Androgen insensitivity syndrome"
        },
        {
          "id": 537312,
          "code": "C1zy000",
          "description": "Pineal gland dysfunction"
        },
        {
          "id": 537313,
          "code": "C1zy100",
          "description": "Progeria"
        },
        {
          "id": 537314,
          "code": "C1zy300",
          "description": "Leprechaunism"
        },
        {
          "id": 537315,
          "code": "C1zy311",
          "description": "Donohue's syndrome"
        },
        {
          "id": 537316,
          "code": "C1zy400",
          "description": "Werner's syndrome"
        },
        {
          "id": 537317,
          "code": "C1zy500",
          "description": "Cyst of pineal gland"
        },
        {
          "id": 537318,
          "code": "C1zy600",
          "description": "Rabson-Mendenhall syndrome"
        },
        {
          "id": 537319,
          "code": "C1zyz11",
          "description": "Werner's syndrome"
        },
        {
          "id": 537320,
          "code": "C28A.00",
          "description": "Vitamin D-dependent rickets"
        },
        {
          "id": 537321,
          "code": "C28A000",
          "description": "Vitamin D-dependent rickets type I"
        },
        {
          "id": 537322,
          "code": "C28A100",
          "description": "Vitamin D-dependent rickets type II"
        },
        {
          "id": 537323,
          "code": "C353.00",
          "description": "Disorders of phosphorus metabolism"
        },
        {
          "id": 537324,
          "code": "C353000",
          "description": "Hypophosphatasia"
        },
        {
          "id": 537325,
          "code": "C353100",
          "description": "Hypophosphatasia rickets"
        },
        {
          "id": 537326,
          "code": "C353200",
          "description": "Vitamin-D-resistant rickets"
        },
        {
          "id": 537327,
          "code": "C353211",
          "description": "Hypophosphataemic rickets"
        },
        {
          "id": 537328,
          "code": "C353500",
          "description": "Acquired hypophosphataemia"
        },
        {
          "id": 537329,
          "code": "C353700",
          "description": "X-linked hypophosphataemic rickets"
        },
        {
          "id": 537330,
          "code": "C353800",
          "description": "Autosomal dominant hypophosphataemic rickets"
        },
        {
          "id": 537331,
          "code": "C353900",
          "description": "Autosomal recessive hypophosphataemic rickets"
        },
        {
          "id": 537332,
          "code": "C353z00",
          "description": "Disorder of phosphorus metabolism NOS"
        },
        {
          "id": 537333,
          "code": "C354.00",
          "description": "Disorders of calcium metabolism"
        },
        {
          "id": 537334,
          "code": "C354200",
          "description": "Idiopathic hypercalcaemia"
        },
        {
          "id": 537335,
          "code": "C354500",
          "description": "Familial benign hypercalcaemia"
        },
        {
          "id": 537336,
          "code": "C354500",
          "description": "Hypercalcaemia familial benign"
        },
        {
          "id": 537337,
          "code": "C354B00",
          "description": "Calciphylaxis"
        },
        {
          "id": 537338,
          "code": "C354D00",
          "description": "Familial hypocalciuric hypercalcaemia"
        },
        {
          "id": 537339,
          "code": "C354y00",
          "description": "Other specified disorder of calcium metabolism"
        },
        {
          "id": 537340,
          "code": "C354z00",
          "description": "Disorder of calcium metabolism NOS"
        },
        {
          "id": 537341,
          "code": "C356.00",
          "description": "Disorders of phosphatases"
        },
        {
          "id": 537342,
          "code": "C36z.11",
          "description": "Liddle's syndrome"
        },
        {
          "id": 537343,
          "code": "Cyu4600",
          "description": "[X]Other adrenogenital disorders"
        },
        {
          "id": 537344,
          "code": "Cyu4900",
          "description": "[X]Other and unspecified primary adrenocortical insufficiency"
        },
        {
          "id": 537345,
          "code": "Cyu4E00",
          "description": "[X]Other polyglandular dysfunction"
        },
        {
          "id": 537346,
          "code": "Cyu4G00",
          "description": "[X]Other hypersecretion of intestinal hormones"
        },
        {
          "id": 537347,
          "code": "F395000",
          "description": "Myopathy due to Addison's disease"
        },
        {
          "id": 537348,
          "code": "F395200",
          "description": "Myopathy due to hypopituitarism"
        },
        {
          "id": 537349,
          "code": "K08yJ00",
          "description": "Pseudohypoaldosteronism"
        },
        {
          "id": 537350,
          "code": "K5B1.00",
          "description": "Female infertility of pituitary - hypothalamic origin"
        },
        {
          "id": 537351,
          "code": "K5B1000",
          "description": "Primary pituitary - hypothalamic infertility"
        },
        {
          "id": 537352,
          "code": "K5B1100",
          "description": "Secondary pituitary - hypothalamic infertility"
        },
        {
          "id": 537353,
          "code": "K5B1z00",
          "description": "Female infertility of pituitary - hypothalamic cause NOS"
        },
        {
          "id": 537354,
          "code": "PK1..00",
          "description": "Anomalies of adrenal gland"
        },
        {
          "id": 537355,
          "code": "PK10.00",
          "description": "Aberrant adrenal gland"
        },
        {
          "id": 537356,
          "code": "PK11.00",
          "description": "Absent adrenal gland"
        },
        {
          "id": 537357,
          "code": "PK12.00",
          "description": "Accessory adrenal gland"
        },
        {
          "id": 537358,
          "code": "PK13.00",
          "description": "Hypoplasia of adrenal gland"
        },
        {
          "id": 537359,
          "code": "PK14.00",
          "description": "Ectopic adrenal gland"
        },
        {
          "id": 537360,
          "code": "PK15.00",
          "description": "Aplasia of adrenal gland"
        },
        {
          "id": 537361,
          "code": "PK1y.00",
          "description": "Other specified anomalies of adrenal gland"
        },
        {
          "id": 537362,
          "code": "PK1y000",
          "description": "Congenital cyst of adrenal gland"
        },
        {
          "id": 537363,
          "code": "PK1yz00",
          "description": "Other congenital anomaly of adrenal gland NOS"
        },
        {
          "id": 537364,
          "code": "PK1z.00",
          "description": "Anomalies of adrenal gland NOS"
        },
        {
          "id": 537365,
          "code": "PK2..00",
          "description": "Other endocrine gland anomalies"
        },
        {
          "id": 537366,
          "code": "PK24.00",
          "description": "Anomalies of pituitary gland"
        },
        {
          "id": 537367,
          "code": "PK24000",
          "description": "Aberrant pituitary gland"
        },
        {
          "id": 537368,
          "code": "PK24100",
          "description": "Congenital absence of pituitary gland"
        },
        {
          "id": 537369,
          "code": "PK24z00",
          "description": "Anomaly of pituitary gland NOS"
        },
        {
          "id": 537370,
          "code": "PK25.00",
          "description": "Anomalies of thyroid gland NEC"
        },
        {
          "id": 537371,
          "code": "PK25000",
          "description": "Aberrant thyroid gland"
        },
        {
          "id": 537372,
          "code": "PK25011",
          "description": "Retrosternal thyroid gland"
        },
        {
          "id": 537373,
          "code": "PK25100",
          "description": "Congenital absence of thyroid gland"
        },
        {
          "id": 537374,
          "code": "PK25z00",
          "description": "Anomaly of thyroid gland NEC NOS"
        },
        {
          "id": 537375,
          "code": "PK26.00",
          "description": "Anomalies of thyroglossal duct NEC"
        },
        {
          "id": 537376,
          "code": "PK27.00",
          "description": "Anomalies of parathyroid gland NEC"
        },
        {
          "id": 537377,
          "code": "PK27000",
          "description": "Aberrant parathyroid gland"
        },
        {
          "id": 537378,
          "code": "PK27100",
          "description": "Accessory parathyroid gland"
        },
        {
          "id": 537379,
          "code": "PK27z00",
          "description": "Anomaly of parathyroid gland NEC NOS"
        },
        {
          "id": 537380,
          "code": "PK2y.00",
          "description": "Other specified endocrine gland anomaly"
        },
        {
          "id": 537381,
          "code": "PK2z.00",
          "description": "Endocrine gland anomaly NOS"
        },
        {
          "id": 537382,
          "code": "Q433700",
          "description": "Neonatal jaundice with congenital hypothyroidism"
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 11525,
      "version_name": "Other endocrine (excluding diabetes) (Read v2)",
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