{
  "id": 11763,
  "label": "isolated growth hormone deficiency type III",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010615",
  "properties": {
    "xrefs": [
      "DOID:0060875",
      "GARD:0003921",
      "MEDGEN:141630",
      "MESH:C537149",
      "OMIM:307200",
      "Orphanet:231692",
      "SCTID:234533006",
      "UMLS:C0472813"
    ],
    "synonyms": [
      "Fleisher syndrome",
      "X-linked IGHD",
      "X-linked isolated growth hormone deficiency",
      "congenital IGHD type III",
      "congenital isolated GH deficiency type III",
      "congenital isolated growth hormone deficiency type III",
      "isolated growth hormone deficiency type III",
      "isolated growth hormone deficiency, type IIi, with agammaglobulinemia, X-linked recessive",
      "Growth hormone deficiency with hypogammaglobulinemia",
      "IGHD 3",
      "IGHD3",
      "agammaglobulinemia and isolated Growth hormone deficiency, X-linked",
      "hypogammaglobulinemia and isolated Growth hormone deficiency, X-linked",
      "isolated growth hormone deficiency type 3",
      "isolated growth hormone deficiency, type 3",
      "isolated growth hormone deficiency, type III"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 2711,
      "label": "isolated congenital growth hormone deficiency",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        14137
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060870",
          "GARD:0012556",
          "MEDGEN:1843308",
          "MedDRA:10035083",
          "NANDO:2200317",
          "OMIMPS:262400",
          "Orphanet:631",
          "SCTID:2109003",
          "UMLS:C5679572",
          "icd11.foundation:936501166"
        ],
        "synonyms": [
          "ICGHD",
          "congenital IGHD",
          "congenital isolated GH deficiency",
          "congenital isolated growth hormone deficiency",
          "isolated growth hormone deficiency",
          "non-acquired isolated growth hormone deficiency"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          }
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0000050"
    }
  ],
  "children": [
    {
      "id": 18888,
      "label": "short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4075,
        11763
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0016538",
          "Orphanet:632"
        ],
        "categories": [
          {
            "ref": "MONDO:0005039",
            "name": "reproductive system disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0005151",
            "name": "endocrine system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018967"
    }
  ],
  "roots": [
    {
      "id": 2711,
      "label": "isolated congenital growth hormone deficiency"
    }
  ]
}