Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4647
Gene Symbol: MYO7A
MYO7A
CUI: C0011053
Disease: Deafness
Deafness 		0.300 Biomarker 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
CUI: C0011053
Disease: Deafness
Deafness 		0.300 CausalMutation CLINVAR