Autosomal recessive nonsyndromic hearing loss 67

Definition

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LHFPL5 gene.

Also known as autosomal recessive nonsyndromic hearing loss 67 — per MONDO

Also identified as

• DOID 0110518 per MONDO
• MESH C565207 per MONDO
• OMIM 610265 per MONDO
• UMLS C1853223 per MONDO