MYO7A — myosin VIIA | MEDLIB

gene with protein productOMIM: 2769034 заболевания

GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)3

Usher syndrome type 2ORPHA:231178

Rare autosomal dominant non-syndromic sensorineural deafness type DFNAORPHA:90635

Rare autosomal recessive non-syndromic sensorineural deafness type DFNBORPHA:90636

Disease-causing germline mutation(s) (loss of function) in1

Usher syndrome type 1ORPHA:231169

gene with protein productOMIM: 2769034 заболевания

GeneCards ↗Open Targets ↗NCBI Gene ↗OMIM ↗

Ассоциированные заболевания

Герминативная мутация (причина)3

Usher syndrome type 2ORPHA:231178

Rare autosomal dominant non-syndromic sensorineural deafness type DFNAORPHA:90635

Rare autosomal recessive non-syndromic sensorineural deafness type DFNBORPHA:90636

Disease-causing germline mutation(s) (loss of function) in1

Usher syndrome type 1ORPHA:231169