Autosomal recessive nonsyndromic hearing loss 66

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the DCDC2 gene.

Also identified as

• DOID 0110517 per MONDO
• MESH C565701 per MONDO
• OMIM 610212 per MONDO
• UMLS C1857750 per MONDO