{
  "id": 18629,
  "label": "11q22.2q22.3 microdeletion syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018632",
  "properties": {
    "xrefs": [
      "GARD:0021858",
      "MEDGEN:1805294",
      "Orphanet:444002",
      "UMLS:C5680062"
    ],
    "synonyms": [
      "11q22.2-q22.3 deletion syndrome",
      "Del(11)(q22.2q22.3)",
      "monosomy 11q22.2-q22.3",
      "monosomy 11q22.2q22.3"
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "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": 17329,
      "label": "partial deletion of the long arm of chromosome 11",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GTR:AN0100478",
          "GTR:AN0100479",
          "GTR:AN0100480",
          "MEDGEN:419905",
          "MESH:C538296",
          "NCIT:C37312",
          "Orphanet:262092",
          "UMLS:C2931804",
          "icd11.foundation:237602200"
        ],
        "synonyms": [
          "partial deletion of chromosome 11q",
          "partial deletion of the long arm of chromosome type 11",
          "partial monosomy of chromosome 11q",
          "partial monosomy of the long arm of chromosome 11",
          "11q deletion",
          "11q monosomy",
          "Deletion 11q partial",
          "chromosome 11q deletion",
          "chromosome 11q partial deletion",
          "del(11q)",
          "deletion 11q",
          "loss of chromosome 11q",
          "monosomy 11q",
          "monosomy 11q partial",
          "partial monosomy 11q"
        ],
        "definition": "A cytogenetic abnormality that refers to the allelic loss of all or part of the long arm of chromosome 11."
      },
      "child_count": 5,
      "reference_id": "MONDO:0016910"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16087,
      "label": "multiple congenital anomalies/dysmorphic syndrome-intellectual disability"
    },
    {
      "id": 17329,
      "label": "partial deletion of the long arm of chromosome 11"
    }
  ]
}