Skip navigation

Disease Deafness, Autosomal Dominant, Due To Mutation In Myo1a

Name Deafness, Autosomal Dominant, Due To Mutation In Myo1a
Categories Ear-nose-throat disease | Nervous system disease | Signs and symptoms
MeSH® ID C567266

Top ↑ Ancestors

1. DiseasesOtorhinolaryngologic Diseases Has associated chemicals Has associated genes Has associated exposure references Ear Diseases Has associated chemicals Has associated genes Has associated exposure references Hearing Disorders Has associated chemicals Has associated genes Has associated exposure references Hearing Loss Has associated chemicals Has associated genes Has associated exposure references Deafness, Autosomal Dominant, Due To Mutation In Myo1a
2. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neurologic Manifestations Has associated chemicals Has associated genes Has associated exposure references Sensation Disorders Has associated chemicals Has associated genes Has associated exposure references Hearing Disorders Has associated chemicals Has associated genes Has associated exposure references Hearing Loss Has associated chemicals Has associated genes Has associated exposure references Deafness, Autosomal Dominant, Due To Mutation In Myo1a
3. DiseasesPathological Conditions, Signs and Symptoms Has associated chemicals Has associated genes Has associated exposure references Signs and Symptoms Has associated chemicals Has associated genes Has associated exposure references Neurologic Manifestations Has associated chemicals Has associated genes Has associated exposure references Sensation Disorders Has associated chemicals Has associated genes Has associated exposure references Hearing Disorders Has associated chemicals Has associated genes Has associated exposure references Hearing Loss Has associated chemicals Has associated genes Has associated exposure references Deafness, Autosomal Dominant, Due To Mutation In Myo1a

Top ↑ Descendants

None.