{
  "id": 18281,
  "label": "neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018131",
  "properties": {
    "xrefs": [
      "GARD:0021526",
      "MEDGEN:1842292",
      "Orphanet:352665",
      "UMLS:C5679925"
    ],
    "synonyms": [
      "9q21 microdeletion syndrome",
      "Del(9)(q21)"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 17327,
      "label": "partial monosomy of the long arm of chromosome 9",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17299
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1826024",
          "Orphanet:262074",
          "UMLS:C5679677",
          "icd11.foundation:1051626600"
        ],
        "synonyms": [
          "partial deletion of chromosome 9q",
          "partial deletion of the long arm of chromosome 9",
          "partial monosomy of chromosome 9q",
          "partial monosomy of the long arm of chromosome type 9"
        ]
      },
      "child_count": 6,
      "reference_id": "MONDO:0016908"
    },
    {
      "id": 18672,
      "label": "neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4427,
        16087,
        18362,
        24488
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017785",
          "Orphanet:453499"
        ],
        "synonyms": [
          "neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 8,
      "reference_id": "MONDO:0018681"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 17327,
      "label": "partial monosomy of the long arm of chromosome 9"
    },
    {
      "id": 18672,
      "label": "neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome"
    }
  ]
}