{
  "concept_id": 4166,
  "concept_version_id": 11526,
  "coding_system": {
    "id": 9,
    "name": "SNOMED  CT codes",
    "description": "SNOMED CT codes"
  },
  "name": "Other endocrine (excluding diabetes) (SNOMED-CT)",
  "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": 9993,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "text/csv",
      "codes": [
        {
          "id": 537383,
          "code": "10340008",
          "description": "Isolated gonadotropin deficiency (disorder)"
        },
        {
          "id": 537384,
          "code": "10680005",
          "description": "Insulin receptor defect (disorder)"
        },
        {
          "id": 537385,
          "code": "111307005",
          "description": "Leprechaunism syndrome (disorder)"
        },
        {
          "id": 537386,
          "code": "111544009",
          "description": "Combination of endocrine dysfunction (disorder)"
        },
        {
          "id": 537387,
          "code": "111546006",
          "description": "Polyglandular dysfunction (disorder)"
        },
        {
          "id": 537388,
          "code": "111551000",
          "description": "Testicular hypofunction (disorder)"
        },
        {
          "id": 537389,
          "code": "111564004",
          "description": "Epinephrine deficiency (disorder)"
        },
        {
          "id": 537390,
          "code": "111569009",
          "description": "Hyperthermia-hyperphagia-hypothyroidism syndrome (disorder)"
        },
        {
          "id": 537391,
          "code": "11244009",
          "description": "Polyglandular autoimmune syndrome, type 1 (disorder)"
        },
        {
          "id": 537392,
          "code": "122811000119101",
          "description": "Partial androgen insensitivity syndrome (disorder)"
        },
        {
          "id": 537393,
          "code": "12313004",
          "description": "Androgen resistance syndrome (disorder)"
        },
        {
          "id": 537394,
          "code": "12331003",
          "description": "Gigantism due to somatostatin deficiency (disorder)"
        },
        {
          "id": 537395,
          "code": "123757009",
          "description": "Complex gonadal endocrine disorder (disorder)"
        },
        {
          "id": 537396,
          "code": "123760002",
          "description": "Prepuberal panhypopituitarism (disorder)"
        },
        {
          "id": 537397,
          "code": "123953004",
          "description": "Idiopathic hypogonadotropic hypogonadism (disorder)"
        },
        {
          "id": 537398,
          "code": "124214007",
          "description": "Deficiency of steroid 11-beta-monooxygenase (disorder)"
        },
        {
          "id": 537399,
          "code": "124220008",
          "description": "Deficiency of steroid 17-alpha-monooxygenase (disorder)"
        },
        {
          "id": 537400,
          "code": "124221007",
          "description": "Deficiency of steroid 21-monooxygenase (disorder)"
        },
        {
          "id": 537401,
          "code": "12427005",
          "description": "Congenital primary adrenocortical hypofunction (disorder)"
        },
        {
          "id": 537402,
          "code": "127009005",
          "description": "Disorder of endocrine receptor (disorder)"
        },
        {
          "id": 537403,
          "code": "128470003",
          "description": "Pineal gland disorder (disorder)"
        },
        {
          "id": 537404,
          "code": "129634000",
          "description": "Induced male hypogonadism syndrome (disorder)"
        },
        {
          "id": 537405,
          "code": "13901000119100",
          "description": "Hypocalciuric hypercalcemia (disorder)"
        },
        {
          "id": 537406,
          "code": "14289006",
          "description": "Myopathy in hypopituitarism (disorder)"
        },
        {
          "id": 537407,
          "code": "15991002",
          "description": "Severe steroid 21-hydroxylase deficiency (disorder)"
        },
        {
          "id": 537408,
          "code": "16685009",
          "description": "Hypocortisolism secondary to another disorder (disorder)"
        },
        {
          "id": 537409,
          "code": "17151000119108",
          "description": "Partial growth hormone deficiency (disorder)"
        },
        {
          "id": 537410,
          "code": "17318002",
          "description": "Virilizing syndrome of adrenal origin (disorder)"
        },
        {
          "id": 537411,
          "code": "178456000",
          "description": "Ateliotic dwarfism without insulinopenia (disorder)"
        },
        {
          "id": 537412,
          "code": "17885001",
          "description": "Iodotyrosine deiodination defect (disorder)"
        },
        {
          "id": 537413,
          "code": "18200000",
          "description": "Autosomal recessive isolated somatotropin deficiency (disorder)"
        },
        {
          "id": 537414,
          "code": "190268003",
          "description": "Congenital hypothyroidism (disorder)"
        },
        {
          "id": 537415,
          "code": "190304001",
          "description": "Dyshormonogenic goiter (disorder)"
        },
        {
          "id": 537416,
          "code": "190470005",
          "description": "Idiopathic panhypopituitarism (disorder)"
        },
        {
          "id": 537417,
          "code": "190472002",
          "description": "Post-infarction panhypopituitarism (disorder)"
        },
        {
          "id": 537418,
          "code": "190480009",
          "description": "Follicle stimulating hormone deficiency (disorder)"
        },
        {
          "id": 537419,
          "code": "190481008",
          "description": "Luteinizing hormone deficiency (disorder)"
        },
        {
          "id": 537420,
          "code": "190512008",
          "description": "Acquired adrenogenital syndrome (disorder)"
        },
        {
          "id": 537421,
          "code": "190859005",
          "description": "Hypophosphatasia (disorder)"
        },
        {
          "id": 537422,
          "code": "190860000",
          "description": "Hypophosphatasia rickets (disorder)"
        },
        {
          "id": 537423,
          "code": "190866006",
          "description": "Idiopathic hypercalcemia (disorder)"
        },
        {
          "id": 537424,
          "code": "193440001",
          "description": "Testicular lesion of adrenogenital syndrome (disorder)"
        },
        {
          "id": 537425,
          "code": "198448006",
          "description": "Female infertility of pituitary - hypothalamic origin (disorder)"
        },
        {
          "id": 537426,
          "code": "198449003",
          "description": "Primary pituitary - hypothalamic infertility (disorder)"
        },
        {
          "id": 537427,
          "code": "198450003",
          "description": "Secondary pituitary - hypothalamic infertility (disorder)"
        },
        {
          "id": 537428,
          "code": "2041006",
          "description": "Eunuchoid gigantism (disorder)"
        },
        {
          "id": 537429,
          "code": "205744006",
          "description": "Congenital cyst of adrenal gland (disorder)"
        },
        {
          "id": 537430,
          "code": "205749001",
          "description": "Congenital absence of pituitary gland (disorder)"
        },
        {
          "id": 537431,
          "code": "205757003",
          "description": "Aberrant parathyroid gland (disorder)"
        },
        {
          "id": 537432,
          "code": "206457007",
          "description": "Neonatal jaundice with congenital hypothyroidism (disorder)"
        },
        {
          "id": 537433,
          "code": "20900005",
          "description": "Nonfamilial asexual dwarfism (disorder)"
        },
        {
          "id": 537434,
          "code": "2109003",
          "description": "Isolated somatotropin deficiency (disorder)"
        },
        {
          "id": 537435,
          "code": "21279007",
          "description": "Lingual thyroid (disorder)"
        },
        {
          "id": 537436,
          "code": "215677009",
          "description": "Congenital hypothyroidism with ectopic thyroid (disorder)"
        },
        {
          "id": 537437,
          "code": "21731004",
          "description": "Female pseudopuberty (disorder)"
        },
        {
          "id": 537438,
          "code": "217710005",
          "description": "Congenital iodine deficiency syndrome (disorder)"
        },
        {
          "id": 537439,
          "code": "22306000",
          "description": "Transient somatotropin deficiency (disorder)"
        },
        {
          "id": 537440,
          "code": "2241003",
          "description": "X-linked absence of thyroxine-binding globulin (disorder)"
        },
        {
          "id": 537441,
          "code": "2243000",
          "description": "Hypercalcemia due to hyperthyroidism (disorder)"
        },
        {
          "id": 537442,
          "code": "22450000",
          "description": "Hyperphosphaturia (disorder)"
        },
        {
          "id": 537443,
          "code": "22558005",
          "description": "Iodide transport defect (disorder)"
        },
        {
          "id": 537444,
          "code": "230581008",
          "description": "Neuropathy in acromegaly (disorder)"
        },
        {
          "id": 537445,
          "code": "230795009",
          "description": "Pituitary coma (disorder)"
        },
        {
          "id": 537446,
          "code": "23536000",
          "description": "Iodotyrosyl coupling defect (disorder)"
        },
        {
          "id": 537447,
          "code": "236464008",
          "description": "Hyporeninemic hypoaldosteronism (disorder)"
        },
        {
          "id": 537448,
          "code": "236796004",
          "description": "Hypogonadism with prune belly syndrome (disorder)"
        },
        {
          "id": 537449,
          "code": "236798003",
          "description": "Androgen resistance - infertile male (disorder)"
        },
        {
          "id": 537450,
          "code": "236811002",
          "description": "Acquired testicular failure (disorder)"
        },
        {
          "id": 537451,
          "code": "237515009",
          "description": "Congenital hypothyroidism without goiter (disorder)"
        },
        {
          "id": 537452,
          "code": "237516005",
          "description": "Congenital thyroid hypoplasia (disorder)"
        },
        {
          "id": 537453,
          "code": "237517001",
          "description": "Congenital atrophy of thyroid (disorder)"
        },
        {
          "id": 537454,
          "code": "237554005",
          "description": "Familial dyshormonogenetic goiter (disorder)"
        },
        {
          "id": 537455,
          "code": "237555006",
          "description": "Hypothyroidism due to iodide trapping defect (disorder)"
        },
        {
          "id": 537456,
          "code": "237556007",
          "description": "Hypothyroidism due to iodide organification defect (disorder)"
        },
        {
          "id": 537457,
          "code": "237559000",
          "description": "Thyroid hormone resistance syndrome (disorder)"
        },
        {
          "id": 537458,
          "code": "237560005",
          "description": "Generalized thyroid hormone resistance (disorder)"
        },
        {
          "id": 537459,
          "code": "237565000",
          "description": "Congenital iodine deficiency syndrome - mixed type (disorder)"
        },
        {
          "id": 537460,
          "code": "237566004",
          "description": "Congenital iodine deficiency syndrome - neurological type (disorder)"
        },
        {
          "id": 537461,
          "code": "237583008",
          "description": "Abnormality of cholecystokinin-pancreozymin secretion (disorder)"
        },
        {
          "id": 537462,
          "code": "237584002",
          "description": "Excessive cholecystokinin-pancreozymin secretion (disorder)"
        },
        {
          "id": 537463,
          "code": "237585001",
          "description": "Abnormality of gastric inhibitory peptide secretion (disorder)"
        },
        {
          "id": 537464,
          "code": "237586000",
          "description": "Excessive gastric inhibitory peptide secretion (disorder)"
        },
        {
          "id": 537465,
          "code": "237587009",
          "description": "Abnormality of glicentin secretion (disorder)"
        },
        {
          "id": 537466,
          "code": "237590003",
          "description": "Abnormality of motilin secretion (disorder)"
        },
        {
          "id": 537467,
          "code": "237591004",
          "description": "Excessive motilin secretion (disorder)"
        },
        {
          "id": 537468,
          "code": "237592006",
          "description": "Abnormality of bombesin secretion (disorder)"
        },
        {
          "id": 537469,
          "code": "237593001",
          "description": "Excessive bombesin secretion (disorder)"
        },
        {
          "id": 537470,
          "code": "237594007",
          "description": "Abnormality of serotonin secretion (disorder)"
        },
        {
          "id": 537471,
          "code": "237595008",
          "description": "Abnormality of neurotensine secretion (disorder)"
        },
        {
          "id": 537472,
          "code": "237674009",
          "description": "Anterior pituitary hyperplasia (disorder)"
        },
        {
          "id": 537473,
          "code": "237682009",
          "description": "Panhypopituitarism - anterior and posterior (disorder)"
        },
        {
          "id": 537474,
          "code": "237683004",
          "description": "Panhypopituitarism - X-linked (disorder)"
        },
        {
          "id": 537475,
          "code": "237684005",
          "description": "Sheehan's syndrome (disorder)"
        },
        {
          "id": 537476,
          "code": "237685006",
          "description": "Partial hypopituitarism (disorder)"
        },
        {
          "id": 537477,
          "code": "237687003",
          "description": "Isolated growth hormone deficiency - autosomal dominant (disorder)"
        },
        {
          "id": 537478,
          "code": "237688008",
          "description": "Idiopathic growth hormone deficiency (disorder)"
        },
        {
          "id": 537479,
          "code": "237689000",
          "description": "Growth hormone neurosecretory dysfunction (disorder)"
        },
        {
          "id": 537480,
          "code": "237691008",
          "description": "Psychosocial growth hormone deficiency (disorder)"
        },
        {
          "id": 537481,
          "code": "237692001",
          "description": "Adrenocorticotropic hormone deficiency (disorder)"
        },
        {
          "id": 537482,
          "code": "237693006",
          "description": "Idiopathic adrenocorticotropic hormone deficiency (disorder)"
        },
        {
          "id": 537483,
          "code": "237699005",
          "description": "Post-traumatic hypopituitarism (disorder)"
        },
        {
          "id": 537484,
          "code": "237700006",
          "description": "Hypopituitarism due to iron overload (disorder)"
        },
        {
          "id": 537485,
          "code": "237701005",
          "description": "Pituitary apoplexy (disorder)"
        },
        {
          "id": 537486,
          "code": "237738005",
          "description": "Alcohol-induced pseudo-Cushing's syndrome (disorder)"
        },
        {
          "id": 537487,
          "code": "237739002",
          "description": "Pseudo-Cushing's syndrome of depression (disorder)"
        },
        {
          "id": 537488,
          "code": "237743003",
          "description": "Glucocorticoid-suppressible hyperaldosteronism (disorder)"
        },
        {
          "id": 537489,
          "code": "237747002",
          "description": "Feminization-adrenogenital syndrome (disorder)"
        },
        {
          "id": 537490,
          "code": "237748007",
          "description": "Pseudohermaphrodite, male with adrenocortical disorder (disorder)"
        },
        {
          "id": 537491,
          "code": "237749004",
          "description": "Virilization-adrenogenital syndrome (disorder)"
        },
        {
          "id": 537492,
          "code": "237750004",
          "description": "Pseudohermaphrodite, female with adrenocortical disorder (disorder)"
        },
        {
          "id": 537493,
          "code": "237751000",
          "description": "Congenital adrenal hyperplasia (disorder)"
        },
        {
          "id": 537494,
          "code": "237753002",
          "description": "Salt-losing congenital adrenal hyperplasia (disorder)"
        },
        {
          "id": 537495,
          "code": "237754008",
          "description": "Late onset congenital adrenal hyperplasia (disorder)"
        },
        {
          "id": 537496,
          "code": "237755009",
          "description": "Congenital adrenal hyperplasia - desmolase deficiency (disorder)"
        },
        {
          "id": 537497,
          "code": "237760008",
          "description": "Addison's disease with adrenoleucodystrophy (disorder)"
        },
        {
          "id": 537498,
          "code": "237761007",
          "description": "Adrenal insufficiency due to adrenal metastasis (disorder)"
        },
        {
          "id": 537499,
          "code": "237762000",
          "description": "Post-adrenalectomy adrenal insufficiency (disorder)"
        },
        {
          "id": 537500,
          "code": "237764004",
          "description": "Congenital adrenal hypoplasia, X-linked (disorder)"
        },
        {
          "id": 537501,
          "code": "237765003",
          "description": "Hyperreninemic hypoaldosteronism (disorder)"
        },
        {
          "id": 537502,
          "code": "237772002",
          "description": "Adrenal atrophy (disorder)"
        },
        {
          "id": 537503,
          "code": "237774001",
          "description": "Small adrenal gland (disorder)"
        },
        {
          "id": 537504,
          "code": "237785004",
          "description": "Hypoadrenalism (disorder)"
        },
        {
          "id": 537505,
          "code": "237786003",
          "description": "Gynecological endocrinology disorder (disorder)"
        },
        {
          "id": 537506,
          "code": "237793004",
          "description": "Hyperandrogenization syndrome (disorder)"
        },
        {
          "id": 537507,
          "code": "237796007",
          "description": "Virilizing adrenal tumor (disorder)"
        },
        {
          "id": 537508,
          "code": "237806007",
          "description": "Androgen receptor absent (disorder)"
        },
        {
          "id": 537509,
          "code": "237807003",
          "description": "Undervirilization (disorder)"
        },
        {
          "id": 537510,
          "code": "237810005",
          "description": "Feminization due to tumor (disorder)"
        },
        {
          "id": 537511,
          "code": "237819006",
          "description": "Pseudo-puberty - virilization (disorder)"
        },
        {
          "id": 537512,
          "code": "237820000",
          "description": "Pseudo-puberty - feminization (disorder)"
        },
        {
          "id": 537513,
          "code": "237822008",
          "description": "Autoimmune endocrine disease (disorder)"
        },
        {
          "id": 537514,
          "code": "237827002",
          "description": "Polyglandular hyperfunction (disorder)"
        },
        {
          "id": 537515,
          "code": "237830009",
          "description": "Ectopic parathyroid hormone-related protein secretion (disorder)"
        },
        {
          "id": 537516,
          "code": "237833006",
          "description": "Carcinoid crisis (disorder)"
        },
        {
          "id": 537517,
          "code": "237839005",
          "description": "Growth hormone receptor abnormality (disorder)"
        },
        {
          "id": 537518,
          "code": "237879001",
          "description": "Disorder of phosphate, calcium and vitamin D metabolism (disorder)"
        },
        {
          "id": 537519,
          "code": "237885008",
          "description": "Familial hypocalciuric hypercalcemia (disorder)"
        },
        {
          "id": 537520,
          "code": "237885008",
          "description": "Familial hypocalciuric hypercalcemia (disorder)"
        },
        {
          "id": 537521,
          "code": "237885008",
          "description": "Familial hypocalciuric hypercalcemia (disorder)"
        },
        {
          "id": 537522,
          "code": "237886009",
          "description": "Familial idiopathic hypercalciuria (disorder)"
        },
        {
          "id": 537523,
          "code": "237889002",
          "description": "Autosomal dominant hypophosphatemic rickets (disorder)"
        },
        {
          "id": 537524,
          "code": "237890006",
          "description": "Autosomal dominant hypophosphatemic bone disease (disorder)"
        },
        {
          "id": 537525,
          "code": "237891005",
          "description": "Autosomal recessive hypophosphatemic bone disease (disorder)"
        },
        {
          "id": 537526,
          "code": "237894002",
          "description": "Vitamin D-dependent rickets type II with alopecia (disorder)"
        },
        {
          "id": 537527,
          "code": "237895001",
          "description": "Vitamin D-dependent rickets type II without alopecia (disorder)"
        },
        {
          "id": 537528,
          "code": "237900002",
          "description": "Calciphylaxis (disorder)"
        },
        {
          "id": 537529,
          "code": "237923004",
          "description": "Dopamine beta-hydroxylase deficiency (disorder)"
        },
        {
          "id": 537530,
          "code": "238870004",
          "description": "Hutchinson-Gilford syndrome (disorder)"
        },
        {
          "id": 537531,
          "code": "238874008",
          "description": "Neonatal pseudo-hydrocephalic progeroid syndrome (disorder)"
        },
        {
          "id": 537532,
          "code": "24867002",
          "description": "Severe adrenal insufficiency (disorder)"
        },
        {
          "id": 537533,
          "code": "250591000119109",
          "description": "Salt-losing congenital adrenal hyperplasia with virilism (disorder)"
        },
        {
          "id": 537534,
          "code": "254255007",
          "description": "Congenital malformation of anterior pituitary (disorder)"
        },
        {
          "id": 537535,
          "code": "254256008",
          "description": "Congenital malformation of posterior pituitary (disorder)"
        },
        {
          "id": 537536,
          "code": "255040004",
          "description": "Parathyroid hormone-related peptide-secreting tumor (disorder)"
        },
        {
          "id": 537537,
          "code": "267386008",
          "description": "Gigantism and acromegaly (disorder)"
        },
        {
          "id": 537538,
          "code": "267388009",
          "description": "Idiopathic hypopituitarism (disorder)"
        },
        {
          "id": 537539,
          "code": "267389001",
          "description": "Post-birth injury hypopituitarism (disorder)"
        },
        {
          "id": 537540,
          "code": "267390005",
          "description": "Post-infarction hypopituitarism (disorder)"
        },
        {
          "id": 537541,
          "code": "267395000",
          "description": "Adrenogenital disorder (disorder)"
        },
        {
          "id": 537542,
          "code": "267402007",
          "description": "Testicular hypofunction due to defect in adrenocortical hormone synthesis (disorder)"
        },
        {
          "id": 537543,
          "code": "267403002",
          "description": "Eunuchism (disorder)"
        },
        {
          "id": 537544,
          "code": "268302006",
          "description": "Aberrant thyroid gland (disorder)"
        },
        {
          "id": 537545,
          "code": "26935004",
          "description": "Tuberculosis of thyroid gland (disorder)"
        },
        {
          "id": 537546,
          "code": "269387007",
          "description": "Testicular lesion in androgen insensitivity syndrome (disorder)"
        },
        {
          "id": 537547,
          "code": "270369000",
          "description": "Stromal cell hyperplasia in androgen insensitivity syndrome (disorder)"
        },
        {
          "id": 537548,
          "code": "271077003",
          "description": "Adrenal virilism (disorder)"
        },
        {
          "id": 537549,
          "code": "271386001",
          "description": "Post-infective hypopituitarism (disorder)"
        },
        {
          "id": 537550,
          "code": "27270004",
          "description": "Pituitary dwarfism with large sella turcica (disorder)"
        },
        {
          "id": 537551,
          "code": "276634002",
          "description": "Idiopathic hyperphosphatasemia (disorder)"
        },
        {
          "id": 537552,
          "code": "276646003",
          "description": "Idiopathic infantile hypercalcemia - mild form (disorder)"
        },
        {
          "id": 537553,
          "code": "276856001",
          "description": "Endocrine andrology disorder (disorder)"
        },
        {
          "id": 537554,
          "code": "27713005",
          "description": "Arthropathy associated with acromegaly (disorder)"
        },
        {
          "id": 537555,
          "code": "277481003",
          "description": "Idiopathic infantile hypercalcemia - severe form (disorder)"
        },
        {
          "id": 537556,
          "code": "277872000",
          "description": "Precocious puberty with adrenal hyperplasia (disorder)"
        },
        {
          "id": 537557,
          "code": "277939004",
          "description": "Chronic myopathy with hypocalcemia and hypophosphatemia (disorder)"
        },
        {
          "id": 537558,
          "code": "277939004",
          "description": "Chronic myopathy with hypocalcemia and hypophosphatemia (disorder)"
        },
        {
          "id": 537559,
          "code": "278503003",
          "description": "Congenital hypothyroidism with diffuse goiter (disorder)"
        },
        {
          "id": 537560,
          "code": "2851000119101",
          "description": "Anterior pituitary hormone deficiency (disorder)"
        },
        {
          "id": 537561,
          "code": "290653008",
          "description": "Postpartum hypopituitarism (disorder)"
        },
        {
          "id": 537562,
          "code": "297267009",
          "description": "Retrosternal thyroid gland (disorder)"
        },
        {
          "id": 537563,
          "code": "30174008",
          "description": "Childhood hypophosphatasia (disorder)"
        },
        {
          "id": 537564,
          "code": "303138003",
          "description": "Thyroglossal duct anomaly (disorder)"
        },
        {
          "id": 537565,
          "code": "308894004",
          "description": "Adrenal necrosis (disorder)"
        },
        {
          "id": 537566,
          "code": "31337009",
          "description": "Feminizing syndrome of adrenal origin (disorder)"
        },
        {
          "id": 537567,
          "code": "32390006",
          "description": "Panhypopituitarism (disorder)"
        },
        {
          "id": 537568,
          "code": "32454003",
          "description": "Congenital anomaly of the thyroid gland (disorder)"
        },
        {
          "id": 537569,
          "code": "32454003",
          "description": "Congenital anomaly of the thyroid gland (disorder)"
        },
        {
          "id": 537570,
          "code": "33559001",
          "description": "Pineal hyperplasia AND diabetes mellitus syndrome (disorder)"
        },
        {
          "id": 537571,
          "code": "33927004",
          "description": "Hypogonadotropic hypogonadism (disorder)"
        },
        {
          "id": 537572,
          "code": "33982008",
          "description": "Hyperphosphatasemia with intellectual disability (disorder)"
        },
        {
          "id": 537573,
          "code": "34041001",
          "description": "Achard-Thiers syndrome (disorder)"
        },
        {
          "id": 537574,
          "code": "34253008",
          "description": "Myopathy in Addison's disease (disorder)"
        },
        {
          "id": 537575,
          "code": "35567006",
          "description": "Isosexual precocious pseudopuberty (disorder)"
        },
        {
          "id": 537576,
          "code": "35868009",
          "description": "Carcinoid syndrome (disorder)"
        },
        {
          "id": 537577,
          "code": "360348000",
          "description": "Pituitary thyroid hormone resistance (disorder)"
        },
        {
          "id": 537578,
          "code": "363627009",
          "description": "Parathyromatosis (disorder)"
        },
        {
          "id": 537579,
          "code": "363732003",
          "description": "Addison's disease (disorder)"
        },
        {
          "id": 537580,
          "code": "3652007",
          "description": "Overproduction of growth hormone (disorder)"
        },
        {
          "id": 537581,
          "code": "367460001",
          "description": "Pituitary dwarfism (disorder)"
        },
        {
          "id": 537582,
          "code": "367524008",
          "description": "Hypoplasia of thyroid (disorder)"
        },
        {
          "id": 537583,
          "code": "368851000119102",
          "description": "Complete androgen insensitivity syndrome (disorder)"
        },
        {
          "id": 537584,
          "code": "370997001",
          "description": "Primary testicular failure (disorder)"
        },
        {
          "id": 537585,
          "code": "371118004",
          "description": "Congenital anomaly of endocrine gonad (disorder)"
        },
        {
          "id": 537586,
          "code": "373662000",
          "description": "Primary adrenocortical insufficiency (disorder)"
        },
        {
          "id": 537587,
          "code": "37495007",
          "description": "Familial adrenocortical hypoplasia (disorder)"
        },
        {
          "id": 537588,
          "code": "38576000",
          "description": "Nonfamilial hyperinsulinemic isolated somatotropin deficiency (disorder)"
        },
        {
          "id": 537589,
          "code": "386584007",
          "description": "Adrenal cortical hypofunction (disorder)"
        },
        {
          "id": 537590,
          "code": "386635007",
          "description": "Precocious puberty with adrenocortical hyperfunction (disorder)"
        },
        {
          "id": 537591,
          "code": "38825009",
          "description": "Deficiency of testosterone biosynthesis (disorder)"
        },
        {
          "id": 537592,
          "code": "39591000119109",
          "description": "Female infertility due to disorder of pituitary gland (disorder)"
        },
        {
          "id": 537593,
          "code": "397827003",
          "description": "Growth hormone deficiency (disorder)"
        },
        {
          "id": 537594,
          "code": "399959003",
          "description": "Premature aging syndrome (disorder)"
        },
        {
          "id": 537595,
          "code": "403254007",
          "description": "Hypermelanosis due to acromegaly (disorder)"
        },
        {
          "id": 537596,
          "code": "40781006",
          "description": "Hypopituitarism due to pituitary tumor (disorder)"
        },
        {
          "id": 537597,
          "code": "408539000",
          "description": "Insulin autoimmune syndrome (disorder)"
        },
        {
          "id": 537598,
          "code": "413099000",
          "description": "Cyst of pineal gland (disorder)"
        },
        {
          "id": 537599,
          "code": "4184009",
          "description": "Congenital anomaly of endocrine gland (disorder)"
        },
        {
          "id": 537600,
          "code": "4184009",
          "description": "Congenital anomaly of endocrine gland (disorder)"
        },
        {
          "id": 537601,
          "code": "4184009",
          "description": "Congenital anomaly of endocrine gland (disorder)"
        },
        {
          "id": 537602,
          "code": "41864002",
          "description": "Autoimmune polyendocrinopathy (disorder)"
        },
        {
          "id": 537603,
          "code": "420351005",
          "description": "Adult-onset growth hormone deficiency (disorder)"
        },
        {
          "id": 537604,
          "code": "420499009",
          "description": "Hypogonadotropic hypogonadism due to isolated gonadotropin deficiency (disorder)"
        },
        {
          "id": 537605,
          "code": "421019006",
          "description": "Hypogonadotropic hypogonadism due to follicle-stimulating hormone deficiency (disorder)"
        },
        {
          "id": 537606,
          "code": "421684006",
          "description": "Adult growth hormone deficiency (disorder)"
        },
        {
          "id": 537607,
          "code": "421821002",
          "description": "Hypogonadotropic hypogonadism due to luteinizing hormone deficiency (disorder)"
        },
        {
          "id": 537608,
          "code": "421931005",
          "description": "Adult growth hormone deficiency with onset in childhood (disorder)"
        },
        {
          "id": 537609,
          "code": "426898004",
          "description": "Virilized female due to gestational hyperandrogenism (disorder)"
        },
        {
          "id": 537610,
          "code": "427627006",
          "description": "Maternal virilization due to placental aromatase deficiency (disorder)"
        },
        {
          "id": 537611,
          "code": "429514007",
          "description": "Growth hormone deficiency after bone marrow transplant (disorder)"
        },
        {
          "id": 537612,
          "code": "43941006",
          "description": "Pseudohypoaldosteronism, type 1 (disorder)"
        },
        {
          "id": 537613,
          "code": "440092001",
          "description": "Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)"
        },
        {
          "id": 537614,
          "code": "442001",
          "description": "Secondary hypopituitarism (disorder)"
        },
        {
          "id": 537615,
          "code": "44231009",
          "description": "Cholesterol monooxygenase (side-chain cleaving) deficiency (disorder)"
        },
        {
          "id": 537616,
          "code": "442498002",
          "description": "Endocrine axis dysfunction (disorder)"
        },
        {
          "id": 537617,
          "code": "442761002",
          "description": "Hypothalamic-pituitary-gonadal axis dysfunction (disorder)"
        },
        {
          "id": 537618,
          "code": "443898004",
          "description": "Virilization of female due to SOX9 gene duplication (disorder)"
        },
        {
          "id": 537619,
          "code": "444058005",
          "description": "Virilization of female due to SRY gene translocation (disorder)"
        },
        {
          "id": 537620,
          "code": "444173008",
          "description": "Undervirilization of male due to steroidogenic acute regulatory protein deficiency (disorder)"
        },
        {
          "id": 537621,
          "code": "449730005",
          "description": "Autoimmune polyendocrine syndrome type 4 (disorder)"
        },
        {
          "id": 537622,
          "code": "449731009",
          "description": "Autoimmune polyendocrine syndrome type 3 (disorder)"
        },
        {
          "id": 537623,
          "code": "45235005",
          "description": "Mild steroid 21-hydroxylase deficiency (disorder)"
        },
        {
          "id": 537624,
          "code": "45248009",
          "description": "Isosexual virilization (disorder)"
        },
        {
          "id": 537625,
          "code": "45414006",
          "description": "Glucocorticoid deficiency with achalasia (disorder)"
        },
        {
          "id": 537626,
          "code": "47757001",
          "description": "Corticosterone 18-monooxygenase deficiency (disorder)"
        },
        {
          "id": 537627,
          "code": "48723006",
          "description": "Male hypogonadism (disorder)"
        },
        {
          "id": 537628,
          "code": "4900002",
          "description": "Endocrine disorder related to puberty (disorder)"
        },
        {
          "id": 537629,
          "code": "49013001",
          "description": "17 alpha-Hydroxyprogesterone aldolase deficiency (disorder)"
        },
        {
          "id": 537630,
          "code": "49494003",
          "description": "Ectopic adrenal gland (disorder)"
        },
        {
          "id": 537631,
          "code": "49494003",
          "description": "Ectopic adrenal gland (disorder)"
        },
        {
          "id": 537632,
          "code": "50029007",
          "description": "Familial hypomagnesemia-hypercalciuria (disorder)"
        },
        {
          "id": 537633,
          "code": "50375007",
          "description": "Thyroid hormone responsiveness defect (disorder)"
        },
        {
          "id": 537634,
          "code": "50658006",
          "description": "Testosterone 17-beta-dehydrogenase deficiency (disorder)"
        },
        {
          "id": 537635,
          "code": "51080000",
          "description": "Complete testicular feminization syndrome (disorder)"
        },
        {
          "id": 537636,
          "code": "51371005",
          "description": "Pituitary dwarfism with normal somatotropin level AND low somatomedin (disorder)"
        },
        {
          "id": 537637,
          "code": "51626007",
          "description": "Werner syndrome (disorder)"
        },
        {
          "id": 537638,
          "code": "52604008",
          "description": "Steroid 21-monooxygenase deficiency, simple virilizing type (disorder)"
        },
        {
          "id": 537639,
          "code": "52832001",
          "description": "Testicular feminization (disorder)"
        },
        {
          "id": 537640,
          "code": "54470008",
          "description": "3 beta-Hydroxysteroid dehydrogenase deficiency (disorder)"
        },
        {
          "id": 537641,
          "code": "55003009",
          "description": "Adrenal medullary insufficiency (disorder)"
        },
        {
          "id": 537642,
          "code": "55236002",
          "description": "Infantile hypophosphatasia (disorder)"
        },
        {
          "id": 537643,
          "code": "56041007",
          "description": "Hypothyroidism due to defect in thyroid hormone synthesis (disorder)"
        },
        {
          "id": 537644,
          "code": "56811006",
          "description": "Pseudohypophosphatasia (disorder)"
        },
        {
          "id": 537645,
          "code": "57863006",
          "description": "Acid phosphatase deficiency (disorder)"
        },
        {
          "id": 537646,
          "code": "59572000",
          "description": "Necrosis of pituitary (disorder)"
        },
        {
          "id": 537647,
          "code": "60045007",
          "description": "Moderate steroid 21-hydroxylase deficiency (disorder)"
        },
        {
          "id": 537648,
          "code": "60086000",
          "description": "Aldosterone deficiency (disorder)"
        },
        {
          "id": 537649,
          "code": "60138009",
          "description": "Anemia of pituitary deficiency (disorder)"
        },
        {
          "id": 537650,
          "code": "60637003",
          "description": "Congenital anomaly of adrenal gland (disorder)"
        },
        {
          "id": 537651,
          "code": "60637003",
          "description": "Congenital anomaly of adrenal gland (disorder)"
        },
        {
          "id": 537652,
          "code": "60637003",
          "description": "Congenital anomaly of adrenal gland (disorder)"
        },
        {
          "id": 537653,
          "code": "60637003",
          "description": "Congenital anomaly of adrenal gland (disorder)"
        },
        {
          "id": 537654,
          "code": "63127008",
          "description": "Thyroglobulin synthesis defect (disorder)"
        },
        {
          "id": 537655,
          "code": "64491003",
          "description": "Myxedematous form of cretinism (disorder)"
        },
        {
          "id": 537656,
          "code": "65048006",
          "description": "Accessory parathyroid gland (disorder)"
        },
        {
          "id": 537657,
          "code": "65274008",
          "description": "Congenital anomaly of parathyroid glands (disorder)"
        },
        {
          "id": 537658,
          "code": "65274008",
          "description": "Congenital anomaly of parathyroid glands (disorder)"
        },
        {
          "id": 537659,
          "code": "6537000",
          "description": "Ectopic pituitary tissue (disorder)"
        },
        {
          "id": 537660,
          "code": "66266003",
          "description": "Phosphopenic type rickets (disorder)"
        },
        {
          "id": 537661,
          "code": "66841006",
          "description": "Mullerian inhibiting factor deficiency (disorder)"
        },
        {
          "id": 537662,
          "code": "66957007",
          "description": "Iatrogenic testicular hypofunction (disorder)"
        },
        {
          "id": 537663,
          "code": "67049004",
          "description": "Vitamin D-dependent rickets, type 1 (disorder)"
        },
        {
          "id": 537664,
          "code": "67528009",
          "description": "Incomplete testicular feminization syndrome (disorder)"
        },
        {
          "id": 537665,
          "code": "67873006",
          "description": "Isolated prolactin deficiency (disorder)"
        },
        {
          "id": 537666,
          "code": "68295002",
          "description": "Vitamin D-dependent rickets (disorder)"
        },
        {
          "id": 537667,
          "code": "68352004",
          "description": "Accessory adrenal gland (disorder)"
        },
        {
          "id": 537668,
          "code": "698854006",
          "description": "Hyperandrogenism due to non-classic type of 21-hydroxylase deficiency (disorder)"
        },
        {
          "id": 537669,
          "code": "699000000",
          "description": "Thyroglossal duct sinus (disorder)"
        },
        {
          "id": 537670,
          "code": "700107006",
          "description": "Bartter syndrome antenatal type 1 (disorder)"
        },
        {
          "id": 537671,
          "code": "700109009",
          "description": "Bartter syndrome antenatal type 2 (disorder)"
        },
        {
          "id": 537672,
          "code": "700111000",
          "description": "Bartter syndrome type 3 (disorder)"
        },
        {
          "id": 537673,
          "code": "700112007",
          "description": "Bartter syndrome type 4 (disorder)"
        },
        {
          "id": 537674,
          "code": "70140000",
          "description": "Receptor-positive androgen resistance syndrome (disorder)"
        },
        {
          "id": 537675,
          "code": "702327009",
          "description": "Monocarboxylate transporter 8 deficiency (disorder)"
        },
        {
          "id": 537676,
          "code": "702614000",
          "description": "Aplasia of parathyroid gland (disorder)"
        },
        {
          "id": 537677,
          "code": "702615004",
          "description": "Aplasia of adrenal gland (disorder)"
        },
        {
          "id": 537678,
          "code": "70348004",
          "description": "Pendred's syndrome (disorder)"
        },
        {
          "id": 537679,
          "code": "704166007",
          "description": "Acquired hypocalciuric hypercalcemia (disorder)"
        },
        {
          "id": 537680,
          "code": "707742001",
          "description": "Bartter syndrome (disorder)"
        },
        {
          "id": 537681,
          "code": "707747007",
          "description": "Pseudoprimary hyperaldosteronism (disorder)"
        },
        {
          "id": 537682,
          "code": "708672004",
          "description": "Odontohypophosphatasia (disorder)"
        },
        {
          "id": 537683,
          "code": "709556009",
          "description": "Periodontitis co-occurrent with hypophosphatasia (disorder)"
        },
        {
          "id": 537684,
          "code": "71003000",
          "description": "Ateleiotic dwarfism (disorder)"
        },
        {
          "id": 537685,
          "code": "715343000",
          "description": "Familial aldosterone deficiency (disorder)"
        },
        {
          "id": 537686,
          "code": "715402001",
          "description": "Hereditary glucocorticoid resistance (disorder)"
        },
        {
          "id": 537687,
          "code": "715633008",
          "description": "Atypical Werner syndrome (disorder)"
        },
        {
          "id": 537688,
          "code": "715668008",
          "description": "Pituitary deficiency due to empty sella turcica syndrome (disorder)"
        },
        {
          "id": 537689,
          "code": "715733000",
          "description": "Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency (disorder)"
        },
        {
          "id": 537690,
          "code": "715734006",
          "description": "Congenital absence of half of thyroid (disorder)"
        },
        {
          "id": 537691,
          "code": "71578002",
          "description": "Steroid 21-monooxygenase deficiency, salt wasting type (disorder)"
        },
        {
          "id": 537692,
          "code": "716338001",
          "description": "Muscular pseudohypertrophy and hypothyroidism syndrome (disorder)"
        },
        {
          "id": 537693,
          "code": "71638002",
          "description": "Disorder of calcium metabolism (disorder)"
        },
        {
          "id": 537694,
          "code": "71638002",
          "description": "Disorder of calcium metabolism (disorder)"
        },
        {
          "id": 537695,
          "code": "71638002",
          "description": "Disorder of calcium metabolism (disorder)"
        },
        {
          "id": 537696,
          "code": "717260007",
          "description": "Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency (disorder)"
        },
        {
          "id": 537697,
          "code": "717261006",
          "description": "Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (disorder)"
        },
        {
          "id": 537698,
          "code": "717334008",
          "description": "Idiopathic congenital hypothyroidism (disorder)"
        },
        {
          "id": 537699,
          "code": "717791000",
          "description": "Bartter syndrome type 4a (disorder)"
        },
        {
          "id": 537700,
          "code": "717897007",
          "description": "Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland (disorder)"
        },
        {
          "id": 537701,
          "code": "718182008",
          "description": "Combined pituitary hormone deficiency genetic form (disorder)"
        },
        {
          "id": 537702,
          "code": "718183003",
          "description": "Familial thyroid dyshormonogenesis (disorder)"
        },
        {
          "id": 537703,
          "code": "718193005",
          "description": "Peripheral resistance to thyroid hormone (disorder)"
        },
        {
          "id": 537704,
          "code": "718194004",
          "description": "Hypothyroidism due to mutation in transcription factor of pituitary development (disorder)"
        },
        {
          "id": 537705,
          "code": "718194004",
          "description": "Hypothyroidism due to mutation in transcription factor of pituitary development (disorder)"
        },
        {
          "id": 537706,
          "code": "718690009",
          "description": "Congenital hypothyroidism due to absence of thyroid gland (disorder)"
        },
        {
          "id": 537707,
          "code": "719451006",
          "description": "Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder)"
        },
        {
          "id": 537708,
          "code": "721233005",
          "description": "Hypergonadotropic hypogonadism with cataract syndrome (disorder)"
        },
        {
          "id": 537709,
          "code": "721842008",
          "description": "Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome (disorder)"
        },
        {
          "id": 537710,
          "code": "721846006",
          "description": "Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder)"
        },
        {
          "id": 537711,
          "code": "722027009",
          "description": "Kallman syndrome with heart disease (disorder)"
        },
        {
          "id": 537712,
          "code": "722288007",
          "description": "Autoimmune enteropathy and endocrinopathy with susceptibility to chronic infection syndrome (disorder)"
        },
        {
          "id": 537713,
          "code": "722375007",
          "description": "Bamforth Lazarus syndrome (disorder)"
        },
        {
          "id": 537714,
          "code": "722380003",
          "description": "Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome (disorder)"
        },
        {
          "id": 537715,
          "code": "722938007",
          "description": "Congenital central hypothyroidism (disorder)"
        },
        {
          "id": 537716,
          "code": "722939004",
          "description": "Congenital hypothyroidism due to iodine deficiency (disorder)"
        },
        {
          "id": 537717,
          "code": "722944006",
          "description": "Congenital hypogonadotropic hypogonadism (disorder)"
        },
        {
          "id": 537718,
          "code": "722947004",
          "description": "Hypocalcemic rickets (disorder)"
        },
        {
          "id": 537719,
          "code": "723999009",
          "description": "Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder)"
        },
        {
          "id": 537720,
          "code": "724097003",
          "description": "Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder)"
        },
        {
          "id": 537721,
          "code": "724275005",
          "description": "Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency (disorder)"
        },
        {
          "id": 537722,
          "code": "724276006",
          "description": "X-linked immune dysregulation, polyendocrinopathy, enteropathy syndrome (disorder)"
        },
        {
          "id": 537723,
          "code": "724385009",
          "description": "Growth delay due to insulin-like growth factor type 1 deficiency (disorder)"
        },
        {
          "id": 537724,
          "code": "725033008",
          "description": "Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (disorder)"
        },
        {
          "id": 537725,
          "code": "725393000",
          "description": "Autosomal dominant primary hypomagnesemia with hypocalciuria (disorder)"
        },
        {
          "id": 537726,
          "code": "725462002",
          "description": "Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency (disorder)"
        },
        {
          "id": 537727,
          "code": "726081005",
          "description": "Hereditary hypophosphatemic rickets with hypercalciuria (disorder)"
        },
        {
          "id": 537728,
          "code": "726081005",
          "description": "Hereditary hypophosphatemic rickets with hypercalciuria (disorder)"
        },
        {
          "id": 537729,
          "code": "72831007",
          "description": "Vitamin D-dependent rickets, type 2 (disorder)"
        },
        {
          "id": 537730,
          "code": "7322007",
          "description": "Accessory adrenal cortex (disorder)"
        },
        {
          "id": 537731,
          "code": "73291005",
          "description": "Congenital absence of parathyroid gland (disorder)"
        },
        {
          "id": 537732,
          "code": "733113002",
          "description": "Hypogonadotropic hypogonadism retinitis pigmentosa syndrome (disorder)"
        },
        {
          "id": 537733,
          "code": "734884008",
          "description": "Diarrhea co-occurrent and due to carcinoid syndrome (disorder)"
        },
        {
          "id": 537734,
          "code": "738771004",
          "description": "Male pseudohermaphroditism due to 5-alpha-reductase deficiency (disorder)"
        },
        {
          "id": 537735,
          "code": "74012004",
          "description": "Congenital anomaly of pituitary gland (disorder)"
        },
        {
          "id": 537736,
          "code": "74012004",
          "description": "Congenital anomaly of pituitary gland (disorder)"
        },
        {
          "id": 537737,
          "code": "74107003",
          "description": "Acromegaly (disorder)"
        },
        {
          "id": 537738,
          "code": "74728003",
          "description": "Hypopituitarism (disorder)"
        },
        {
          "id": 537739,
          "code": "75065003",
          "description": "Endemic cretinism (disorder)"
        },
        {
          "id": 537740,
          "code": "7530009",
          "description": "Asexual dwarfism (disorder)"
        },
        {
          "id": 537741,
          "code": "75667007",
          "description": "Lingual goiter (disorder)"
        },
        {
          "id": 537742,
          "code": "758664007",
          "description": "Isolated follicle stimulating hormone deficiency (disorder)"
        },
        {
          "id": 537743,
          "code": "763311001",
          "description": "Adrenomyodystrophy (disorder)"
        },
        {
          "id": 537744,
          "code": "763890006",
          "description": "Short stature with delayed bone age due to thyroid hormone metabolism deficiency (disorder)"
        },
        {
          "id": 537745,
          "code": "764960005",
          "description": "Inherited isolated adrenal insufficiency due to partial cytochrome P450 family 11 subfamily A member 1 deficiency (disorder)"
        },
        {
          "id": 537746,
          "code": "7651000119100",
          "description": "Mineralocorticoid deficiency (disorder)"
        },
        {
          "id": 537747,
          "code": "765326001",
          "description": "Familial glucocorticoid deficiency (disorder)"
        },
        {
          "id": 537748,
          "code": "76556008",
          "description": "Hyperphosphatasia-osteoectasia syndrome (disorder)"
        },
        {
          "id": 537749,
          "code": "766817004",
          "description": "Short stature due to growth hormone secretagogue receptor deficiency (disorder)"
        },
        {
          "id": 537750,
          "code": "766986002",
          "description": "Acute adrenal insufficiency (disorder)"
        },
        {
          "id": 537751,
          "code": "76715008",
          "description": "Addison's disease due to autoimmunity (disorder)"
        },
        {
          "id": 537752,
          "code": "770567006",
          "description": "Progeroid syndrome Petty type (disorder)"
        },
        {
          "id": 537753,
          "code": "77098009",
          "description": "Pseudohypoaldosteronism (disorder)"
        },
        {
          "id": 537754,
          "code": "771236000",
          "description": "Visceral calciphylaxis (disorder)"
        },
        {
          "id": 537755,
          "code": "771262009",
          "description": "Pseudoleprechaunism syndrome Patterson type (disorder)"
        },
        {
          "id": 537756,
          "code": "771308008",
          "description": "Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome (disorder)"
        },
        {
          "id": 537757,
          "code": "771445001",
          "description": "Autosomal recessive infantile hypercalcemia (disorder)"
        },
        {
          "id": 537758,
          "code": "771510006",
          "description": "X-linked central congenital hypothyroidism with late-onset testicular enlargement (disorder)"
        },
        {
          "id": 537759,
          "code": "773331001",
          "description": "Nestor Guillermo progeria syndrome (disorder)"
        },
        {
          "id": 537760,
          "code": "773406003",
          "description": "Mandibular hypoplasia, deafness, progeroid syndrome (disorder)"
        },
        {
          "id": 537761,
          "code": "773426004",
          "description": "Lamin A/C related cardiocutaneous progeria syndrome (disorder)"
        },
        {
          "id": 537762,
          "code": "773645004",
          "description": "Familial infantile gigantism (disorder)"
        },
        {
          "id": 537763,
          "code": "773664005",
          "description": "Deficiency in anterior pituitary function, variable immunodeficiency syndrome (disorder)"
        },
        {
          "id": 537764,
          "code": "773666007",
          "description": "Hypoinsulinemic hypoglycemia and body hemihypertrophy (disorder)"
        },
        {
          "id": 537765,
          "code": "776417008",
          "description": "Acroosteolysis, keloid-like lesions, premature aging syndrome (disorder)"
        },
        {
          "id": 537766,
          "code": "778005007",
          "description": "Duplication of pituitary gland (disorder)"
        },
        {
          "id": 537767,
          "code": "778064009",
          "description": "Ectopic aldosterone-producing neoplasm (disorder)"
        },
        {
          "id": 537768,
          "code": "782917007",
          "description": "Familial adrenal hypoplasia with absent pituitary luteinizing hormone (disorder)"
        },
        {
          "id": 537769,
          "code": "783008000",
          "description": "Pituitary dermoid and epidermoid cysts (disorder)"
        },
        {
          "id": 537770,
          "code": "783009008",
          "description": "Pituitary deficiency due to Rathke cleft cysts (disorder)"
        },
        {
          "id": 537771,
          "code": "783620009",
          "description": "Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis (disorder)"
        },
        {
          "id": 537772,
          "code": "783696009",
          "description": "Hyperandrogenism due to cortisone reductase deficiency (disorder)"
        },
        {
          "id": 537773,
          "code": "789187001",
          "description": "X-linked acrogigantism due to Xq26 microduplication (disorder)"
        },
        {
          "id": 537774,
          "code": "7990002",
          "description": "Immunoglobulinemia with isolated somatotropin deficiency (disorder)"
        },
        {
          "id": 537775,
          "code": "80599001",
          "description": "Isolated corticotropin deficiency (disorder)"
        },
        {
          "id": 537776,
          "code": "80849007",
          "description": "Gigantism (disorder)"
        },
        {
          "id": 537777,
          "code": "819950002",
          "description": "Generalized glucocorticoid resistance syndrome (disorder)"
        },
        {
          "id": 537778,
          "code": "82236004",
          "description": "Familial x-linked hypophosphatemic vitamin D refractory rickets (disorder)"
        },
        {
          "id": 537779,
          "code": "82236004",
          "description": "Familial x-linked hypophosphatemic vitamin D refractory rickets (disorder)"
        },
        {
          "id": 537780,
          "code": "82236004",
          "description": "Familial x-linked hypophosphatemic vitamin D refractory rickets (disorder)"
        },
        {
          "id": 537781,
          "code": "82560004",
          "description": "Leydig cell failure in adult (disorder)"
        },
        {
          "id": 537782,
          "code": "83190008",
          "description": "Congenital absence of adrenal gland (disorder)"
        },
        {
          "id": 537783,
          "code": "83190008",
          "description": "Congenital absence of adrenal gland (disorder)"
        },
        {
          "id": 537784,
          "code": "83728000",
          "description": "Polyglandular autoimmune syndrome, type 2 (disorder)"
        },
        {
          "id": 537785,
          "code": "838322007",
          "description": "Autonomic neuropathy due to Allgrove syndrome (disorder)"
        },
        {
          "id": 537786,
          "code": "840473004",
          "description": "Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form (disorder)"
        },
        {
          "id": 537787,
          "code": "840474005",
          "description": "Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency non classic form (disorder)"
        },
        {
          "id": 537788,
          "code": "840509001",
          "description": "Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form (disorder)"
        },
        {
          "id": 537789,
          "code": "846680003",
          "description": "Functional hypogonadotropic hypogonadism (disorder)"
        },
        {
          "id": 537790,
          "code": "84781002",
          "description": "Sporadic cretinism (disorder)"
        },
        {
          "id": 537791,
          "code": "85096001",
          "description": "Adrenal infarction (disorder)"
        },
        {
          "id": 537792,
          "code": "85487008",
          "description": "Renal phosphaturia (disorder)"
        },
        {
          "id": 537793,
          "code": "85880000",
          "description": "Pseudohypoaldosteronism, type 1, dominant form (disorder)"
        },
        {
          "id": 537794,
          "code": "86073008",
          "description": "Hypersomatotropic gigantism (disorder)"
        },
        {
          "id": 537795,
          "code": "860796007",
          "description": "Hyperphosphatemic familial tumoral calcinosis (disorder)"
        },
        {
          "id": 537796,
          "code": "86353007",
          "description": "Hypocalciuria (disorder)"
        },
        {
          "id": 537797,
          "code": "87049008",
          "description": "Disorder of phosphorus metabolism (disorder)"
        },
        {
          "id": 537798,
          "code": "87049008",
          "description": "Disorder of phosphorus metabolism (disorder)"
        },
        {
          "id": 537799,
          "code": "87049008",
          "description": "Disorder of phosphorus metabolism (disorder)"
        },
        {
          "id": 537800,
          "code": "8829008",
          "description": "Isolated lutropin deficiency (disorder)"
        },
        {
          "id": 537801,
          "code": "8868001",
          "description": "Dyshormonogenetic goiter AND iodide leak (disorder)"
        },
        {
          "id": 537802,
          "code": "89476005",
          "description": "Pituitary cachexia (disorder)"
        },
        {
          "id": 537803,
          "code": "90505000",
          "description": "Autosomal recessive hypophosphatemic vitamin D refractory rickets (disorder)"
        },
        {
          "id": 537804,
          "code": "91187007",
          "description": "Pituitary dwarfism with small sella turcica (disorder)"
        },
        {
          "id": 537805,
          "code": "91285009",
          "description": "Ectopic adrenal cortex (disorder)"
        },
        {
          "id": 537806,
          "code": "91632005",
          "description": "Hypophosphaturia (disorder)"
        },
        {
          "id": 537807,
          "code": "92978002",
          "description": "Congenital absence of thyroid gland (disorder)"
        },
        {
          "id": 537808,
          "code": "93068008",
          "description": "Congenital hypertrophy of adrenal gland (disorder)"
        },
        {
          "id": 537809,
          "code": "93235007",
          "description": "Congenital hypoplasia of adrenal gland (disorder)"
        },
        {
          "id": 537810,
          "code": "9526000",
          "description": "Pineal gland dysfunction (disorder)"
        },
        {
          "id": 537811,
          "code": "95622006",
          "description": "Fetal virilism (disorder)"
        },
        {
          "id": 537812,
          "code": "95830009",
          "description": "Pituitary infarction (disorder)"
        },
        {
          "id": 537813,
          "code": "9979004",
          "description": "Disorder of androgen receptor (disorder)"
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 11526,
      "version_name": "Other endocrine (excluding diabetes) (SNOMED-CT)",
      "version_date": "2025-01-19T16:42:43.402626Z",
      "is_published": true,
      "is_latest": true
    }
  ]
}