{
  "id": 17222,
  "label": "paternal 14q32.2 microdeletion syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016780",
  "properties": {
    "xrefs": [
      "GARD:0017220",
      "MEDGEN:1842589",
      "Orphanet:254525",
      "UMLS:C5679639"
    ],
    "synonyms": [
      "paternal del(14)(q32.2)",
      "paternal monosomy 14q32.2"
    ],
    "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"
    },
    {
      "id": 17331,
      "label": "partial deletion of the long arm of chromosome 14",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3128
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:444119",
          "Orphanet:262110",
          "UMLS:C2931697"
        ],
        "synonyms": [
          "partial deletion of chromosome 14q",
          "partial deletion of the long arm of chromosome type 14",
          "partial monosomy of chromosome 14q",
          "partial monosomy of the long arm of chromosome 14",
          "14q deletion",
          "14q monosomy",
          "chromosome 14q deletion",
          "deletion 14q",
          "monosomy 14q",
          "partial monosomy 14q"
        ],
        "definition": "Chromosome 14q deletion is a chromosome abnormality that occurs when there is a missing (deleted) copy of genetic material on the long arm (q) of chromosome 14."
      },
      "child_count": 6,
      "reference_id": "MONDO:0016912"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 15540,
      "label": "motor developmental delay due to 14q32.2 paternally expressed gene defect"
    },
    {
      "id": 17331,
      "label": "partial deletion of the long arm of chromosome 14"
    }
  ]
}