{
  "id": 19584,
  "label": "thyroid hypoplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019861",
  "properties": {
    "xrefs": [
      "GARD:0008426",
      "MEDGEN:57720",
      "MedDRA:10065938",
      "Orphanet:95720",
      "UMLS:C0151516",
      "icd11.foundation:936952450"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ],
    "definition": "Thyroid hypoplasia is a form of thyroid dysgenesis characterized by incomplete development of the thyroid gland that results in primary congenital hypothyroidism, a permanent thyroid deficiency that is present from birth."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10294,
      "label": "generalized resistance to thyroid hormone",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3557,
        6233
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000301",
          "MEDGEN:1654700",
          "Orphanet:3221",
          "UMLS:C4722330"
        ],
        "synonyms": [
          "GRTH",
          "Refetoff syndrome",
          "deafness-thyroid hormone resistance syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A thyroid hormone resistance syndrome characterized by resistance in the pituitary gland and in most or all of the peripheral tissues."
      },
      "child_count": 12,
      "reference_id": "MONDO:0009043"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10294,
      "label": "generalized resistance to thyroid hormone"
    }
  ]
}