MYO5A, myosin VA, 4644

N. diseases: 82; N. variants: 4
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1860157
Disease: Elejalde Disease
Elejalde Disease
0.500 Biomarker disease GENOMICS_ENGLAND Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity. 12148598 2002
CUI: C1860157
Disease: Elejalde Disease
Elejalde Disease
0.500 GermlineCausalMutation disease ORPHANET