{
  "id": 10398,
  "label": "hypothyroidism, congenital, nongoitrous, 5",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009154",
  "properties": {
    "xrefs": [
      "DOID:0070125",
      "GARD:0015165",
      "MEDGEN:388687",
      "MESH:C567123",
      "OMIM:225250",
      "UMLS:C2673630"
    ],
    "synonyms": [
      "CHNG5",
      "NKX2-5 hypothyroidism, congenital, nongoitrous",
      "hypothyroidism, congenital nongoitrous, 5",
      "hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5",
      "hypothyroidism, congenital, nongoitrous, 5",
      "hypothyroidism, congenital, nongoitrous, type 5",
      "congenital nongoitrous hypothyroidism 5"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Any hypothyroidism, congenital, nongoitrous in which the cause of the disease is a mutation in the NKX2-5 gene."
  },
  "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"
    }
  ]
}