Autosomal recessive nonsyndromic hearing loss 98

Definition

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

Also known as autosomal recessive nonsyndromic hearing loss 98 — per MONDO

Also identified as

• DOID 0110540 per MONDO
• OMIM 614861 per MONDO
• UMLS C3553932 per MONDO