{
  "id": 10374,
  "label": "Dyggve-Melchior-Clausen disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009130",
  "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."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 17206,
      "label": "spondyloepiphyseal dysplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7171
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112280",
          "GARD:0007687",
          "ICD10CM:Q77.7",
          "ICD9:756.9",
          "MEDGEN:20916",
          "MedDRA:10062920",
          "Orphanet:252",
          "UMLS:C0038015"
        ],
        "synonyms": [
          "SED",
          "spondyloepiphyseal dysplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An osteochondrodysplasia that results in abnormalities of bone growth in the vertebral column and the epiphysis."
      },
      "child_count": 44,
      "reference_id": "MONDO:0016761"
    }
  ],
  "children": [
    {
      "id": 11736,
      "label": "Dyggve-Melchior-Clausen syndrome, X-linked",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        2902,
        10374
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 0,
      "reference_id": "MONDO:0010583"
    }
  ],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 17206,
      "label": "spondyloepiphyseal dysplasia"
    }
  ]
}