Nystagmus 1, congenital, X-linked

Definition

Any congenital nystagmus in which the cause of the disease is a mutation in the FRMD7 gene.

Also known as congenital nystagmus caused by mutation in FRMD7, FRMD7 congenital nystagmus, nystagmus 1, congenital, X-linked — per MONDO

Also identified as

• DOID 0111790 per MONDO
• MESH C537853 per MONDO
• OMIM 310700 per MONDO
• UMLS C1839580 per MONDO