Autosomal recessive nonsyndromic hearing loss 68

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the S1PR2 gene.

Also known as autosomal recessive nonsyndromic hearing loss 68 — per MONDO

Also identified as

• DOID 0110519 per MONDO
• MESH C563669 per MONDO
• OMIM 610419 per MONDO
• UMLS C1835854 per MONDO