{
  "id": 12004,
  "label": "tibial muscular dystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010870",
  "properties": {
    "xrefs": [
      "DOID:0111078",
      "GARD:0013154",
      "MEDGEN:333047",
      "OMIM:600334",
      "Orphanet:609",
      "SCTID:698846009",
      "UMLS:C1838244"
    ],
    "synonyms": [
      "Finnish tibial muscular dystrophy",
      "TMD",
      "Udd myopathy",
      "distal myopathy, Udd type",
      "distal titinopathy",
      "tardive tibial muscular dystrophy",
      "Tmd",
      "tibial muscular dystrophy, tardive"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A distal myopathy characterized by weakness of the muscles of the anterior compartment of lower limbs, appearing in the fourth to seventh decade of life."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16734,
      "label": "autosomal dominant distal myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        18871
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020361",
          "MEDGEN:1826097",
          "Orphanet:206650",
          "UMLS:C5680803"
        ],
        "synonyms": [
          "distal myopathy, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal dominant form of distal myopathy."
      },
      "child_count": 30,
      "reference_id": "MONDO:0016108"
    },
    {
      "id": 24220,
      "label": "autosomal dominant titinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        23917
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026247"
        ],
        "synonyms": [
          "TTN-related myopathy, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal dominant form of TTN-related myopathy."
      },
      "child_count": 8,
      "reference_id": "MONDO:0100494"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16734,
      "label": "autosomal dominant distal myopathy"
    },
    {
      "id": 24220,
      "label": "autosomal dominant titinopathy"
    }
  ]
}