Autosomal recessive nonsyndromic hearing loss 23

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the PCDH15 gene.

Also identified as

• DOID 0110481 per MONDO
• MESH C563705 per MONDO
• OMIM 609533 per MONDO
• UMLS C1836027 per MONDO