{
  "id": 22876,
  "label": "congenital-onset Steinert myotonic dystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0035646",
  "properties": {
    "xrefs": [
      "GARD:0022361",
      "ICD10CM:G71.1",
      "Orphanet:589821"
    ],
    "synonyms": [
      "Congenital-onset Steinert disease",
      "Congenital-onset myotonic dystrophy type 1"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 9379,
      "label": "myotonic dystrophy type 1",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16733,
        21518
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:11722",
          "GARD:0008310",
          "ICD9:359.21",
          "MEDGEN:886881",
          "NCIT:C84679",
          "NORD:1075",
          "OMIM:160900",
          "Orphanet:273",
          "UMLS:C3250443",
          "icd11.foundation:557405480"
        ],
        "synonyms": [
          "DM1",
          "DMPK myotonic dystrophy",
          "MD1",
          "Myotonic Dystrophy",
          "Steinert disease",
          "Steinert myotonic dystrophy syndrome",
          "Steinert syndrome",
          "dystrophia myotonica",
          "myotonic dystrophy caused by mutation in DMPK",
          "myotonic dystrophy type 1",
          "Steinert myotonic dystrophy",
          "Steinert's disease",
          "dystrophia myotonica 1",
          "dystrophia myotonica type 1",
          "myotonic dystrophy 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Steinert disease, also known as myotonic dystrophy type 1, is a muscle disease characterized by myotonia and by multiorgan damage that combines various degrees of muscle weakness, arrhythmia and/or cardiac conduction disorders, cataract, endocrine damage, sleep disorders and baldness."
      },
      "child_count": 2,
      "reference_id": "MONDO:0008056"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 9379,
      "label": "myotonic dystrophy type 1"
    }
  ]
}