VCP, valosin containing protein, 7415

N. diseases: 376; N. variants: 25
Disease: Ophthalmoplegia ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		0.010 GeneticVariation phenotype BEFREE VCP myopathy can cause unusual manifestations that include ophthalmoplegia, ptosis, and dysphagia. 30488450 2019