{
  "id": 19665,
  "label": "reducing body myopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0019948",
  "properties": {
    "xrefs": [
      "DOID:0080090",
      "GARD:0012162",
      "ICD9:359.89",
      "MEDGEN:543081",
      "NANDO:2200875",
      "Orphanet:97239",
      "SCTID:42779002",
      "UMLS:C0270970",
      "icd11.foundation:397698784"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "Reducing body myopathy (RBM) is a rare muscle disorder marked by progressive muscle weakness and the presence of characteristic inclusion bodies in affected muscle fibers."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 19669,
      "label": "congenital myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7023,
        24618
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080100",
          "DOID:0081337",
          "GARD:0005898",
          "MEDGEN:124381",
          "MedDRA:10062547",
          "NANDO:1200477",
          "NANDO:2100234",
          "OMIMPS:117000",
          "Orphanet:97245",
          "UMLS:C0270960",
          "icd11.foundation:1185572073"
        ],
        "synonyms": [
          "congenital myopathy",
          "Batten Turner congenital myopathy",
          "myopathy congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 106,
      "reference_id": "MONDO:0019952"
    }
  ],
  "children": [
    {
      "id": 11575,
      "label": "myopathy, reducing body, X-linked, early-onset, severe",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19665,
        25048
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015261",
          "MEDGEN:906731",
          "MESH:C567469",
          "OMIM:300717",
          "UMLS:C4225423"
        ],
        "synonyms": [
          "myopathy, reducing body, X-linked, early-onset, severe",
          "reducing body myopathy, X-linked 1a, severe, infantile or early childhood onset, X-linked dominant",
          "RBMX1A",
          "reducing body myopathy, X-linked 1A, severe, with infantile or early childhood onset"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010414"
    },
    {
      "id": 11576,
      "label": "myopathy, reducing body, X-linked, childhood-onset",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        19665,
        25048
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080687",
          "GARD:0015262",
          "MEDGEN:904593",
          "MESH:C567468",
          "OMIM:300718",
          "UMLS:C4225159"
        ],
        "synonyms": [
          "myopathy, reducing body, X-linked, childhood-onset",
          "RBMX1B",
          "reducing body myopathy, X-linked 1B, with late childhood or adult onset"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010415"
    }
  ],
  "roots": [
    {
      "id": 19669,
      "label": "congenital myopathy"
    }
  ]
}