Autosomal recessive nonsyndromic hearing loss 63

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 63 — per MONDO

Also identified as

• DOID 0110515 per MONDO
• MESH C566951 per MONDO
• OMIM 611451 per MONDO
• UMLS C1969621 per MONDO