Disease phenotype
OMIM
Gene symbol (chromosome)
protein
protein
VCP (9p13-p12)
valosin-containing protein
GNE (9p13.3)
UDP-N-acetylglucosamine-2- epimerase/N-acetylmannosamine kinase
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
|