{
  "id": 11736,
  "label": "Dyggve-Melchior-Clausen syndrome, X-linked",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010583",
  "properties": {
    "xrefs": [
      "GARD:0015290",
      "MEDGEN:337052",
      "OMIM:304950",
      "UMLS:C1844654"
    ],
    "synonyms": [
      "Dyggve-Melchior-Clausen disease, X-linked",
      "Dyggve-Melchior-Clausen syndrome, X-linked",
      "X-linked Dyggve-Melchior-Clausen disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "X-linked form of Dyggve-Melchior-Clausen disease."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2902,
      "label": "X-linked disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050735",
          "ICD9:799.89",
          "MEDGEN:222910",
          "MESH:D040181",
          "NCIT:C85865",
          "SCTID:128430005",
          "UMLS:C1138434"
        ],
        "synonyms": [
          "X-linked disease or disorder",
          "X-linked hereditary disease",
          "X-linked hereditary disorder",
          "X-linked inherited disease",
          "X-linked inherited disorder",
          "disease or disorder, X-linked",
          "disease, X-linked",
          "X linked genetic diseases",
          "X-linked genetic disease",
          "X-linked genetic diseases",
          "disease, X-linked genetic",
          "diseases, X-linked genetic",
          "genetic disease, X-linked",
          "genetic diseases, X chromosome linked",
          "genetic diseases, X linked",
          "genetic diseases, X-chromosome linked"
        ],
        "definition": "X-linked form of disease."
      },
      "child_count": 50,
      "reference_id": "MONDO:0000425"
    },
    {
      "id": 10374,
      "label": "Dyggve-Melchior-Clausen disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        17206
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111167",
          "GARD:0006295",
          "MEDGEN:120527",
          "NCIT:C124844",
          "NORD:1068",
          "OMIM:223800",
          "Orphanet:239",
          "SCTID:82699004",
          "UMLS:C0265286",
          "icd11.foundation:21266164"
        ],
        "synonyms": [
          "Dyggve Melchior Clausen syndrome",
          "Dyggve-Melchior-Clausen disease",
          "Dyggve-Melchior-Clausen syndrome",
          "DMC",
          "DMC syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Dyggve-Melchior-Clausen disease (DMC) is a rare skeletal disorder belonging to the group of spondyloepimetaphyseal dysplasias."
      },
      "child_count": 2,
      "reference_id": "MONDO:0009130"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2902,
      "label": "X-linked disease"
    },
    {
      "id": 10374,
      "label": "Dyggve-Melchior-Clausen disease"
    }
  ]
}