{
  "id": 14292,
  "label": "chromosome 15q24 deletion syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013256",
  "properties": {
    "xrefs": [
      "DECIPHER:66",
      "DOID:0060395",
      "GARD:0012219",
      "MEDGEN:462024",
      "MESH:C579849",
      "OMIM:613406",
      "Orphanet:94065",
      "SCTID:699308002",
      "UMLS:C3150674"
    ],
    "synonyms": [
      "15q24 microdeletion syndrome",
      "15q24 recurrent microdeletion syndrome",
      "Del(15)(q24)",
      "chromosome 15q24 deletion syndrome",
      "monosomy 15q24",
      "WITKOS",
      "Witteveen-Kolk syndrome",
      "chromosome 15Q24 Duplication syndrome"
    ],
    "definition": "15q24 microdeletion syndrome is a rare chromosomal anomaly characterized cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5714,
      "label": "hereditary disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29382
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:630",
          "EFO:0000508",
          "ICD9:799.89",
          "MEDGEN:5527",
          "MESH:D030342",
          "NCIT:C3101",
          "SCTID:32895009",
          "UMLS:C0019247"
        ],
        "synonyms": [
          "genetic condition",
          "genetic disease",
          "genetic disorder",
          "hereditary disease",
          "hereditary disease or disorder",
          "hereditary diseases",
          "inherited disease",
          "inherited genetic disease",
          "molecular disease",
          "Mendelian disease",
          "familial disorder",
          "inborn disorder"
        ],
        "definition": "A disease that is caused by genetic modifications where those modifications are inherited from a parent's genome."
      },
      "child_count": 1925,
      "reference_id": "MONDO:0003847"
    },
    {
      "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": 5714,
      "label": "hereditary disease"
    },
    {
      "id": 16087,
      "label": "multiple congenital anomalies/dysmorphic syndrome-intellectual disability"
    },
    {
      "id": 17332,
      "label": "partial deletion of the long arm of chromosome 15"
    }
  ]
}