{
  "id": 10995,
  "label": "opsismodysplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009785",
  "properties": {
    "xrefs": [
      "GARD:0004098",
      "MEDGEN:140927",
      "MESH:C537122",
      "OMIM:258480",
      "Orphanet:2746",
      "SCTID:254068007",
      "UMLS:C0432219",
      "icd11.foundation:2147268863"
    ],
    "synonyms": [
      "opsismodysplasia",
      "OPSISMODYSPLASIA",
      "OPSMD"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Opsismodysplasia is a skeletal dysplasia characterized by congenital dwarfism and facial dysmorphism."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 24805,
      "label": "severe spondylodysplastic dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19472
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026429"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An instance of spondylodysplastic dysplasia that has a high degree of severity."
      },
      "child_count": 5,
      "reference_id": "MONDO:0800080"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 24805,
      "label": "severe spondylodysplastic dysplasia"
    }
  ]
}