{
  "id": 13412,
  "label": "congenital nongoitrous hypothyroidism 3",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012360",
  "properties": {
    "xrefs": [
      "DOID:0070127",
      "GARD:0024862",
      "MEDGEN:424853",
      "MESH:C567935",
      "OMIM:609893",
      "UMLS:C2940785"
    ],
    "synonyms": [
      "CHNG3",
      "hypothyroidism, congenital, nongoitrous, 3",
      "resistance to thyrotropin",
      "thyrotropin resistance"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "A congenital hypothyroidism characterized by autosomal dominant inheritance of resistance to thyrotropin that has material basis in variation in the chromosome region 15q25.3-q26.1."
  },
  "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"
    },
    {
      "id": 19705,
      "label": "peripheral resistance to thyroid hormones",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16929
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012734",
          "MEDGEN:902322",
          "Orphanet:97927",
          "SCTID:718193005",
          "UMLS:C4273673"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "Peripheral resistance to thyroid hormones may be a cause of permanent congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth."
      },
      "child_count": 2,
      "reference_id": "MONDO:0019995"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2710,
      "label": "hypothyroidism, congenital, nongoitrous"
    },
    {
      "id": 19705,
      "label": "peripheral resistance to thyroid hormones"
    }
  ]
}