{
  "id": 10923,
  "label": "Thomsen and Becker disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009710",
  "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)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 19001,
      "label": "muscular channelopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18957,
        29384
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018917",
          "MEDGEN:1842600",
          "Orphanet:71864",
          "UMLS:C5681306"
        ],
        "synonyms": [
          "channelopathy of muscle tissue",
          "muscle tissue channelopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A channelopathy that involves the muscle tissue."
      },
      "child_count": 24,
      "reference_id": "MONDO:0019119"
    }
  ],
  "children": [
    {
      "id": 9378,
      "label": "myotonia congenita, autosomal dominant",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10923,
        24271
      ],
      "type_id": 0,
      "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"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0008055"
    },
    {
      "id": 10928,
      "label": "myotonia congenita, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7611,
        10923,
        24271
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000844",
          "MEDGEN:155852",
          "NANDO:1200499",
          "OMIM:255700",
          "UMLS:C0751360"
        ],
        "synonyms": [
          "autosomal recessive myotonia congenita",
          "myotonia congenita, autosomal recessive",
          "myotonia congenita, recessive",
          "Becker disease",
          "myotonia, generalised",
          "myotonia, generalized"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal recessive form of myotonia congenita."
      },
      "child_count": 0,
      "reference_id": "MONDO:0009715"
    }
  ],
  "roots": [
    {
      "id": 19001,
      "label": "muscular channelopathy"
    }
  ]
}