autosomal recessive nonsyndromic hearing loss 9
MONDO:0010986Also known as: autosomal recessive nonsyndromic hearing loss 9, DFNB9, NRSD9, OTOF autosomal recessive nonsyndromic deafness, auditory neuropathy, autosomal recessive, 1
- MONDO:
- MONDO:0010986
- OMIM:
- 601071 ↗
Rare disease39 associated genes
Description
Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the OTOF gene.
Associated genes
+29 more genes — install the extension to see the full list inline on any page.