Autosomal recessive nonsyndromic hearing loss 18A

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the USH1C gene.

Also identified as

• DOID 0110473 per MONDO
• MESH C566580 per MONDO
• OMIM 602092 per MONDO
• UMLS C1865870 per MONDO