{
  "id": 26272,
  "label": "3q26q28 deletion syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0979291",
  "properties": {
    "xrefs": [
      "MEDGEN:1882544",
      "Orphanet:695611",
      "UMLS:C6010434"
    ]
  },
  "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": 17321,
      "label": "partial deletion of the long arm of chromosome 3",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17293
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1825968",
          "Orphanet:262019",
          "UMLS:C5679675",
          "icd11.foundation:1054533453"
        ],
        "synonyms": [
          "partial deletion of chromosome 3q",
          "partial deletion of the long arm of chromosome type 3",
          "partial monosomy of chromosome 3q",
          "partial monosomy of the long arm of chromosome 3"
        ]
      },
      "child_count": 5,
      "reference_id": "MONDO:0016902"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16087,
      "label": "multiple congenital anomalies/dysmorphic syndrome-intellectual disability"
    },
    {
      "id": 17321,
      "label": "partial deletion of the long arm of chromosome 3"
    }
  ]
}