Autosomal recessive nonsyndromic hearing loss 59

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 59 — per MONDO

Also identified as

• DOID 0110511 per MONDO
• MESH C565698 per MONDO
• OMIM 610220 per MONDO
• UMLS C1857744 per MONDO