Disease phenotype | OMIM | Gene symbol (chromosome) protein |
| inclusion body myopathy with early-onset paget disease and frontotemporal dement | VCP (9p13-p12) valosin-containing protein | |
| Inclusion body myopathy, autosomal recessive | GNE (9p13.3) UDP-N-acetylglucosamine-2- epimerase/N-acetylmannosamine kinase |