{
  "id": 17051,
  "label": "transient congenital hypothyroidism due to neonatal factor",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016556",
  "properties": {
    "xrefs": [
      "GARD:0020646",
      "MEDGEN:1842815",
      "Orphanet:238699",
      "UMLS:C5680930"
    ],
    "categories": [
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16545,
      "label": "transient congenital hypothyroidism",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18613
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020142",
          "MEDGEN:820541",
          "NCIT:C113171",
          "Orphanet:178045",
          "SCTID:119181000119104",
          "UMLS:C3827793",
          "icd11.foundation:592246939"
        ],
        "synonyms": [
          "THOP",
          "hypothyroxinemia of prematurity",
          "transient hypothyroxinemia of prematurity"
        ],
        "categories": [
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ],
        "definition": "A common, self-limiting thyroid disorder seen in preterm infants that is characterized by abnormally low serum levels of thyroxine and free thyroxine with normal serum levels of thyroid stimulating hormone."
      },
      "child_count": 2,
      "reference_id": "MONDO:0015792"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16545,
      "label": "transient congenital hypothyroidism"
    }
  ]
}