{
  "id": 18888,
  "label": "short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018967",
  "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"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4075,
      "label": "congenital agammaglobulinemia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        10564,
        16629
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:14177",
          "GARD:0023034",
          "ICD9:279.04",
          "MEDGEN:1806025",
          "UMLS:C5574711"
        ],
        "synonyms": [
          "congenital agammaglobulinemia",
          "congenital hypogammaglobulinemia (finding)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ],
        "definition": "An instance of agammaglobulinemia that is present from birth."
      },
      "child_count": 4,
      "reference_id": "MONDO:0001902"
    },
    {
      "id": 11763,
      "label": "isolated growth hormone deficiency type III",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2711
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 1,
      "reference_id": "MONDO:0010615"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4075,
      "label": "congenital agammaglobulinemia"
    },
    {
      "id": 11763,
      "label": "isolated growth hormone deficiency type III"
    }
  ]
}