Autosomal recessive nonsyndromic hearing loss 42

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the ILDR1 gene.

Also known as autosomal recessive nonsyndromic hearing loss 42 — per MONDO

Also identified as

• DOID 0110500 per MONDO
• MESH C566460 per MONDO
• OMIM 609646 per MONDO
• UMLS C1864818 per MONDO