Autosomal dominant nonsyndromic hearing loss 28

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the GRHL2 gene.

Also identified as

• DOID 0110557 per MONDO
• MESH C563890 per MONDO
• OMIM 608641 per MONDO
• UMLS C1837640 per MONDO