{
  "id": 11561,
  "label": "X-linked scapuloperoneal muscular dystrophy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010400",
  "properties": {
    "xrefs": [
      "GARD:0007608",
      "MEDGEN:395530",
      "OMIM:300695",
      "Orphanet:431272",
      "UMLS:C2678061"
    ],
    "synonyms": [
      "X-linked SPMD",
      "X-linked scapuloperoneal syndrome",
      "scapuloperoneal myopathy, X-linked dominant, X-linked dominant",
      "SPM",
      "scapuloperoneal myopathy, FHL1-related",
      "scapuloperoneal myopathy, X-linked dominant"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "X-linked scapuloperoneal muscular dystrophy (X-linked SPMD) is a skeletal muscle disease characterized by late onset, co-occurrence of scapular and peroneal muscle weakness, and scapular winging."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3107,
      "label": "scapuloperoneal myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17256
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060253",
          "GARD:0022820",
          "MEDGEN:419759",
          "MESH:C536624",
          "UMLS:C2931268"
        ],
        "synonyms": [
          "myopathy, scapuloperoneal",
          "scapuloperoneal syndrome, myopathic type"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A muscular dystrophy which begins at the lower legs and affects the shoulder region earlier and more severely than distal arm."
      },
      "child_count": 2,
      "reference_id": "MONDO:0000727"
    },
    {
      "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": 3107,
      "label": "scapuloperoneal myopathy"
    },
    {
      "id": 25048,
      "label": "FHL1-related myopathy"
    }
  ]
}