{
  "id": 21305,
  "label": "hypothyroidism, congenital, nongoitrous, 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024264",
  "properties": {
    "xrefs": [
      "DOID:0070124",
      "GARD:0025378",
      "MEDGEN:358389",
      "MESH:C566852",
      "OMIM:218700",
      "UMLS:C1869118"
    ],
    "synonyms": [
      "CHNG2",
      "hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia",
      "hypothyroidism, congenital, nongoitrous, 2",
      "athyreotic hypothyroidism",
      "congenital nongoitrous hypothyroidism 2",
      "hypothyroidism, athyreotic",
      "hypothyroidism, congenital, due to thyroid dysgenesis",
      "resistance to thyrotropin",
      "thyroid agenesis",
      "thyroid dysgenesis",
      "thyroid hypoplasia",
      "thyroid, ectopic",
      "thyrotropin resistance"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A congenital hypothyroidism that has material basis in heterozygous mutation in the PAX8 gene on chromosome 2q13."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2710,
      "label": "hypothyroidism, congenital, nongoitrous",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        18613
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0022704",
          "OMIMPS:275200"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 18,
      "reference_id": "MONDO:0000045"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2710,
      "label": "hypothyroidism, congenital, nongoitrous"
    }
  ]
}