{
  "id": 8474,
  "label": "Acromicric dysplasia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007055",
  "properties": {
    "xrefs": [
      "DOID:0111243",
      "GARD:0000007",
      "ICD9:756.59",
      "MEDGEN:78549",
      "MESH:C535662",
      "NORD:725",
      "OMIM:102370",
      "Orphanet:969",
      "SCTID:254090007",
      "UMLS:C0265287",
      "icd11.foundation:1006372687"
    ],
    "synonyms": [
      "Acromicric dysplasia",
      "ACMICD",
      "Acromicric skeletal dysplasia"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "A rare bone dysplasia characterized by short stature, short hands and feet, mild facial dysmorphism, and characteristic X-ray abnormalities of the hands."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 19473,
      "label": "acromelic dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18360
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019194",
          "MEDGEN:1843369",
          "Orphanet:93436",
          "UMLS:C4736195",
          "icd11.foundation:177141175"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 18,
      "reference_id": "MONDO:0019695"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 19473,
      "label": "acromelic dysplasia"
    }
  ]
}