eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | inclusion body myositis |
| Comorbidity | C0029401|paget\'s disease |
| Sentences | 4 |
| PubMedID- 24677265 | The mettl21 family of proteins methylates chaperones involved in the etiology of both myopathy and inclusion body myositis with paget's disease. |
| PubMedID- 22644520 | Since valosin-containing protein mutations were reported as a cause of hereditary inclusion body myositis associated with paget's disease of the bone and frontotemporal dementia, many new mutations have been described in the last decade. |
| PubMedID- 24717448 | Found that mutations in the vcp gene result in the autosomal-dominant degenerative disease known as inclusion body myositis with paget's disease of the bone and frontotemporal dementia [54]. |
| PubMedID- 25557955 | In addition, we describe other genetic associations between dementia and neuromuscular disease, such as inclusion body myositis with paget's disease and ftd. |
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