Pharos: autosomal dominant nonsyndromic deafness 17 (1 associated targets)

Disease Summary

Associated Targets (1)

Tbio

GARD Rare

Mondo Description

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the MYH9 gene.

Uniprot Description

A form of deafness characterized by progressive high frequency hearing impairment and cochleosaccular degeneration.

Mondo Term and Equivalent IDs

MONDO:0011350: autosomal dominant nonsyndromic deafness 17

DOID:0110548: autosomal dominant nonsyndromic deafness 17

GARD:0009726:

OMIM:603622: DEAFNESS, AUTOSOMAL DOMINANT 17