Autosomal dominant nonsyndromic hearing loss 41

Definition

Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the P2RX2 gene.

Also identified as

• DOID 0110567 per MONDO
• MESH C564272 per MONDO
• OMIM 608224 per MONDO
• UMLS C1842371 per MONDO