Autosomal recessive nonsyndromic hearing loss 15

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GIPC3 gene.

Also known as autosomal recessive nonsyndromic hearing loss 15 — per MONDO

Also identified as

• DOID 0110470 per MONDO
• MESH C566611 per MONDO
• OMIM 601869 per MONDO
• UMLS C1866094 per MONDO