eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | inclusion body myositis |
| Comorbidity | C0029401|paget\'s disease of the bone |
| Sentences | 2 |
| 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- 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. |
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