{
  "id": 3460,
  "label": "hypoparathyroidism",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0001220",
  "properties": {
    "xrefs": [
      "DOID:11199",
      "EFO:0009451",
      "GARD:0006733",
      "ICD10CM:E20",
      "ICD10WHO:E20",
      "ICD9:252.1",
      "MEDGEN:6985",
      "MESH:D007011",
      "NANDO:1200775",
      "NANDO:2100124",
      "NANDO:2200345",
      "NCIT:C78350",
      "SCTID:36976004",
      "UMLS:C0020626",
      "icd11.foundation:1708733050"
    ],
    "synonyms": [
      "hypoparathyroidism, idiopathic (subtype)",
      "parathyroid, underactivity of"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Hypoparathyroidism is an endocrine disorder in which the parathyroid glands in the neck do not produce enough parathyroid hormone (PTH). Common signs and symptoms include abdominal pain, brittle nails, cataracts, dry hair and skin, muscle cramps, tetany, pain in the face, legs, and feet, seizures, tingling sensation, and weakened tooth enamel (in children). It may be caused by injury to the parathyroid glands (e.g., during surgery). Other causes, include low blood magnesium levels, a side effect of radioactive iodine treatment for hyperthyroidism, metabolic alkalosis, DiGeorge syndrome, and type I polyglandular autoimmune syndrome. The goal of treatment is to restore the calcium and mineral balance in the body."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 3,
  "parents": [
    {
      "id": 3463,
      "label": "parathyroid gland disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6875
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11201",
          "EFO:0005754",
          "ICD9:252",
          "ICD9:252.8",
          "ICD9:252.9",
          "MEDGEN:893009",
          "MESH:D010279",
          "NCIT:C26844",
          "SCTID:73132005",
          "UMLS:C4025822",
          "icd11.foundation:962023213"
        ],
        "synonyms": [
          "disease of parathyroid gland",
          "disease or disorder of parathyroid gland",
          "disorder of parathyroid gland",
          "parathyroid disease",
          "parathyroid gland disease",
          "parathyroid gland disease or disorder",
          "parathyroid gland diseases",
          "parathyroid gland disorder",
          "parathyroid gland disorders"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A disease involving the parathyroid gland."
      },
      "child_count": 4,
      "reference_id": "MONDO:0001223"
    }
  ],
  "children": [
    {
      "id": 16219,
      "label": "secondary hypoparathyroidism due to impaired parathormon secretion",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3460
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019922",
          "MEDGEN:931097",
          "Orphanet:140286",
          "UMLS:C4305428",
          "icd11.foundation:1229357339"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0015357"
    },
    {
      "id": 16764,
      "label": "hereditary hypoparathyroidism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3460,
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020407",
          "MEDGEN:1842344",
          "Orphanet:208593",
          "UMLS:C5680825"
        ],
        "synonyms": [
          "genetic hypoparathyroidism"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "An instance of hypoparathyroidism that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 6,
      "reference_id": "MONDO:0016165"
    },
    {
      "id": 18365,
      "label": "autoimmune hypoparathyroidism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2997,
        3460
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018824",
          "HP:0011771",
          "MEDGEN:488838",
          "Orphanet:36913",
          "SCTID:75316000",
          "UMLS:C0271865",
          "icd11.foundation:1790437089"
        ],
        "synonyms": [
          "autoimmune hypoparathyroidism",
          "autoimmune hypoparathyroidism (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "An autoimmune form of hypoparathyroidism."
      },
      "child_count": 2,
      "reference_id": "MONDO:0018242"
    }
  ],
  "roots": [
    {
      "id": 3463,
      "label": "parathyroid gland disorder"
    }
  ]
}