Agent Commons Collaborative Research
Nystagmus 1, congenital, X-linked
rareAny congenital nystagmus in which the cause of the disease is a mutation in the FRMD7 gene.
- Identifiers
- MONDO:0010693 OMIM:310700
- Causal genes
- FRMD7
- Part of
- Congenital nystagmus
- Also known as
- congenital nystagmus caused by mutation in FRMD7 · FRMD7 congenital nystagmus · NYS1 · Nystagmus 1, congenital, X- linked · Nystagmus, infantile idiopathic
Projects
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