{
  "id": 16731,
  "label": "acquired skeletal muscle disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016105",
  "properties": {
    "xrefs": [
      "MEDGEN:1842576",
      "Orphanet:206638",
      "UMLS:C5680799"
    ],
    "synonyms": [
      "acquired skeletal muscle disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      }
    ],
    "definition": "An instance of skeletal muscle disease that is acquired during the lifetime of the individual."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 19743,
      "label": "skeletal muscle disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5798
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:735900",
          "MedDRA:10028641",
          "Orphanet:98472",
          "SCTID:75047002",
          "UMLS:C1533847"
        ],
        "synonyms": [
          "disease of skeletal muscle tissue",
          "disease or disorder of skeletal muscle tissue",
          "disorder of skeletal muscle tissue",
          "skeletal muscle tissue disease",
          "skeletal muscle tissue disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "A disease involving the skeletal muscle tissue."
      },
      "child_count": 13,
      "reference_id": "MONDO:0020120"
    }
  ],
  "children": [
    {
      "id": 16154,
      "label": "idiopathic camptocormia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16731,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0001063",
          "MEDGEN:120496",
          "MESH:C537968",
          "MedDRA:10069646",
          "Orphanet:1320",
          "SCTID:13534001",
          "UMLS:C0264162"
        ],
        "synonyms": [
          "idiopathic camptocormism",
          "idiopathic progressive lumbar kyphosis",
          "bent spine",
          "bent spine syndrome",
          "camptocormia",
          "camptocormism"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "Idiopathic camptocormia is a postural disease characterized by an anterior flexion of the torso (during walking or standing) that resolves in the supine position and that is caused by weakness of the lumbar paraspinal muscles (spinal extensors), due to massive fatty infiltrations of posterior spinal muscles, without an identifiable etiology."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015271"
    },
    {
      "id": 18646,
      "label": "idiopathic dropped head syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16731,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:1001987",
          "GARD:0021874",
          "Orphanet:447881"
        ],
        "synonyms": [
          "isolated neck extensor myopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018654"
    },
    {
      "id": 18864,
      "label": "macrophagic myofasciitis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16731
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000176",
          "MEDGEN:419858",
          "MESH:C537829",
          "Orphanet:592",
          "SCTID:718175009",
          "UMLS:C2931639"
        ],
        "synonyms": [
          "MMF",
          "Macrophagic myofasciitis, childhood"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018942"
    },
    {
      "id": 19745,
      "label": "acquired idiopathic inflammatory myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16731,
        24391,
        24405
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009128",
          "ICD9:359.79",
          "Orphanet:98482",
          "icd11.foundation:464294586"
        ],
        "synonyms": [
          "IIm",
          "IMM",
          "idiopathic inflammatory myopathies",
          "idiopathic inflammatory myositis",
          "idiopathic inflammatory myopathy, familial"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "An umbrella term for diseases which have chronic muscle inflammation and weakness of unknown etiology. The types of idiopathic inflammatory myopathy are further defined by either clinicopathologic criteria or by the presence of certain autoantibodies."
      },
      "child_count": 27,
      "reference_id": "MONDO:0020122"
    },
    {
      "id": 20379,
      "label": "acquired rippling muscle disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        12729,
        16731
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0025294"
        ],
        "synonyms": [
          "acquired rippling muscle disease",
          "sporadic rippling muscle disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ],
        "definition": "The acquired form of RMD. Although RMD most often is reported with autosomal dominant inheritance, some sporadic cases are found, and an association with other diseases such as myasthenia gravis has also been reported."
      },
      "child_count": 2,
      "reference_id": "MONDO:0021142"
    }
  ],
  "roots": [
    {
      "id": 19743,
      "label": "skeletal muscle disorder"
    }
  ]
}