{
  "id": 13814,
  "label": "chromosome 15q13.3 microdeletion syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012774",
  "properties": {
    "xrefs": [
      "DECIPHER:74",
      "DOID:0060394",
      "GARD:0010296",
      "MEDGEN:393784",
      "MESH:C567439",
      "OMIM:612001",
      "Orphanet:199318",
      "SCTID:699254009",
      "UMLS:C2677613"
    ],
    "synonyms": [
      "15q13.3 microdeletion syndrome",
      "Del(15)(q13.3)",
      "chromosome 15q13.3 microdeletion syndrome",
      "monosomy 15q13.3",
      "15q13.3 microdeletion",
      "chromosome 15q13.3 deletion syndrome",
      "microdeletion 15q13.3 syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "15q13.3 microdeletion (microdel15q13.3) syndrome is characterized by a wide spectrum of neurodevelopmental disorders with no or subtle dysmorphic features."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2490",
          "ICD9:742",
          "MEDGEN:105425",
          "NCIT:C97172",
          "UMLS:C0497552"
        ],
        "synonyms": [
          "congenital abnormality of the nervous system",
          "congenital nervous system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An abnormality of the nervous system that is present at birth or detected in the neonatal period."
      },
      "child_count": 217,
      "reference_id": "MONDO:0002320"
    },
    {
      "id": 16087,
      "label": "multiple congenital anomalies/dysmorphic syndrome-intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18951
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019832",
          "MEDGEN:1826158",
          "Orphanet:102283",
          "UMLS:C5680372"
        ],
        "synonyms": [
          "MCA/MR",
          "multiple congenital anomalies-intellectual disability with or without dysmorphism",
          "multiple congenital anomalies/dysmorphic syndrome-intellectual disability"
        ]
      },
      "child_count": 338,
      "reference_id": "MONDO:0015159"
    },
    {
      "id": 17332,
      "label": "partial deletion of the long arm of chromosome 15",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        3128
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:444123",
          "MESH:C538038",
          "Orphanet:262119",
          "UMLS:C2931708"
        ],
        "synonyms": [
          "partial deletion of chromosome 15q",
          "partial deletion of the long arm of chromosome type 15",
          "partial monosomy of chromosome 15q",
          "partial monosomy of the long arm of chromosome 15",
          "15q deletion",
          "15q monosomy",
          "chromosome 15q deletion",
          "deletion 15q",
          "monosomy 15q",
          "partial monosomy 15q"
        ]
      },
      "child_count": 9,
      "reference_id": "MONDO:0016913"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder"
    },
    {
      "id": 16087,
      "label": "multiple congenital anomalies/dysmorphic syndrome-intellectual disability"
    },
    {
      "id": 17332,
      "label": "partial deletion of the long arm of chromosome 15"
    }
  ]
}