VCP
valosin containing protein
Ассоциированные заболевания
Герминативная мутация (причина)6
Amyotrophic lateral sclerosisORPHA:803
→Frontotemporal dementia with motor neuron diseaseORPHA:275872
→Spastic paraplegia-Paget disease of bone syndromeORPHA:329475
→Adult-onset distal myopathy due to VCP mutationORPHA:329478
→Autosomal dominant Charcot-Marie-Tooth disease type 2YORPHA:435387
→Inclusion body myopathy with Paget disease of bone and frontotemporal dementiaORPHA:52430
→Основной фактор предрасположенности2