Gene: MYO7A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.300 Biomarker phenotype RGD Mutations in human MYO7A result in Usher syndrome type 1B, a severe autosomal inherited recessive disease that involves deafness and vestibular dysfunction. 15965244 2005
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A 		0.300 CausalMutation phenotype CLINVAR