{
  "id": 9378,
  "label": "myotonia congenita, autosomal dominant",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008055",
  "properties": {
    "xrefs": [
      "DOID:0081336",
      "GARD:0006176",
      "ICD9:359.29",
      "MEDGEN:422446",
      "OMIM:160800",
      "SCTID:57938005",
      "SCTID:8960007",
      "UMLS:C2936781"
    ],
    "synonyms": [
      "Thomsen and Becker disease",
      "Thomsen disease",
      "myotonia congenita, autosomal dominant",
      "myotonia congenita, dominant",
      "myotonia Levior"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 10923,
      "label": "Thomsen and Becker disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19001
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2106",
          "GARD:0012301",
          "ICD10CM:G71.12",
          "ICD9:359.22",
          "MESH:D009224",
          "MedDRA:10028655",
          "MedDRA:10043461",
          "NANDO:1200497",
          "NANDO:1200498",
          "NCIT:C84912",
          "Orphanet:614",
          "SCTID:726051002"
        ],
        "synonyms": [
          "myotonia congenita",
          "Batten-Turner congenital myopathy",
          "myopathy, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, genetic, skeletal muscle channelopathy characterized by slow muscle relaxation after contraction (myotonia)."
      },
      "child_count": 2,
      "reference_id": "MONDO:0009710"
    },
    {
      "id": 24271,
      "label": "hereditary neuromuscular disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18957,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026275"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that is characterized by progressive muscle degeneration and weakness."
      },
      "child_count": 44,
      "reference_id": "MONDO:0100546"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 10923,
      "label": "Thomsen and Becker disease"
    },
    {
      "id": 24271,
      "label": "hereditary neuromuscular disease"
    }
  ]
}