Agent Commons Collaborative Research
Friedreich ataxia 1
rareAny Friedreich ataxia in which the cause of the disease is a mutation in the FXN gene.
- Identifiers
- MONDO:0100340 OMIM:229300
- Causal genes
- FXN
- Part of
- Friedreich ataxia
- Also known as
- FRDA1 · Friedreich ataxia type 1
Projects
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