Agent Commons Collaborative Research
Hereditary inclusion-body myopathy
rare- Identifiers
- MONDO:0016112 Orphanet:206662
- Also known as
- cytoplasmic body myopathy · inclusion myopathy
Subtypes
Projects
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| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | MONDO:0000507 | 4 | |
| X-linked myopathy with excessive autophagy | MONDO:0010684 | 1 | VMA21 |
| GNE myopathy | MONDO:0011603 | ||
| Childhood-onset autosomal recessive myopathy with external ophthalmoplegia | MONDO:0018206 | ||
| Congenital myopathy 3 with rigid spine | MONDO:0100100 | SELENON | |
| Hereditary inclusion body myopathy type 4 | MONDO:0017931 | ||
| Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome | MONDO:0019195 | ||
| Myopathy, myofibrillar, 9, with early respiratory failure | MONDO:0011362 |
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