{
  "id": 9557,
  "label": "isolated growth hormone deficiency type II",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008250",
  "properties": {
    "xrefs": [
      "DOID:0060872",
      "GARD:0001696",
      "MEDGEN:124405",
      "MESH:C562704",
      "OMIM:173100",
      "Orphanet:231679",
      "SCTID:237687003",
      "UMLS:C0271567"
    ],
    "synonyms": [
      "congenital IGHD type II",
      "congenital isolated GH deficiency type II",
      "congenital isolated growth hormone deficiency type II",
      "growth hormone deficiency, isolated, type II",
      "Growth hormone deficiency, isolated autosomal dominant",
      "Growth hormone deficiency, isolated, autosomal dominant",
      "IGHD 2",
      "IGHD2",
      "isolated Growth hormone deficiency, type 2",
      "isolated growth hormone deficiency type 2",
      "isolated growth hormone deficiency, type II",
      "pituitary dwarfism due to isolated Growth hormone deficiency, autosomal dominant",
      "pituitary dwarfism due to isolated growth hormone deficiency autosomal dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0005039",
        "name": "reproductive system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0005151",
        "name": "endocrine system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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": [],
  "roots": [
    {
      "id": 2711,
      "label": "isolated congenital growth hormone deficiency"
    }
  ]
}