Autosomal recessive nonsyndromic hearing loss 25

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the GRXCR1 gene.

Also known as autosomal recessive nonsyndromic hearing loss 25 — per MONDO

Also identified as

• DOID 0110483 per MONDO
• OMIM 613285 per MONDO
• UMLS C1414017 per MONDO