{
  "id": 17224,
  "label": "paternal 14q32.2 hypomethylation syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016782",
  "properties": {
    "xrefs": [
      "GARD:0017222",
      "MEDGEN:1842839",
      "Orphanet:254531",
      "UMLS:C5680721"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 15540,
      "label": "motor developmental delay due to 14q32.2 paternally expressed gene defect",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111713",
          "GARD:0013431",
          "MEDGEN:863995",
          "NCIT:C120409",
          "OMIM:616222",
          "Orphanet:254516",
          "UMLS:C4015558"
        ],
        "synonyms": [
          "mUPD14 syndrome",
          "maternal uniparental disomy chromosome 14 syndrome",
          "TEMPLE syndrome",
          "uniparental disomy, maternal, chromosome 14"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A cause of obesity that results from inheritance of two copies of chromosome 14 from the mother, and no copy of chromosome 14 from the father."
      },
      "child_count": 3,
      "reference_id": "MONDO:0014541"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 15540,
      "label": "motor developmental delay due to 14q32.2 paternally expressed gene defect"
    }
  ]
}