{
  "id": 11464,
  "label": "Uruguay Faciocardiomusculoskeletal syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010292",
  "properties": {
    "xrefs": [
      "DOID:0112148",
      "GARD:0024717",
      "MEDGEN:335320",
      "MESH:C564544",
      "OMIM:300280",
      "UMLS:C1846010"
    ],
    "synonyms": [
      "Uruguay Faciocardiomusculoskeletal syndrome",
      "uruguay faciocardiomusculoskeletal syndrome, X-linked recessive",
      "FCMSU",
      "Fcms",
      "URUGUAY FACIOCARDIOMUSCULOSKELETAL syndrome",
      "faciocardiomusculoskeletal syndrome, Uruguay type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 25048,
      "label": "FHL1-related myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7023,
        24618
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026563"
        ],
        "synonyms": [
          "FHL1-related myopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A group of myopathies that includes Emery-Dreifuss muscular dystrophy (EDMD), and two allelic disorders characterized by the presence of reducing body on histopathology, namely reducing body myopathy (RBM) and scapuloperoneal myopathy."
      },
      "child_count": 10,
      "reference_id": "MONDO:0800462"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 25048,
      "label": "FHL1-related myopathy"
    }
  ]
}