Autosomal dominant nonsyndromic hearing loss 25

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the SLC17A8 gene.

Also identified as

• DOID 0110555 per MONDO
• MESH C565319 per MONDO
• OMIM 605583 per MONDO
• UMLS C1854158 per MONDO