Friedreich ataxia 1
MONDO:0100340Any Friedreich ataxia in which the cause of the disease is a mutation in the FXN gene.
Also known as: Friedreich ataxia, FRDA1, Friedreich ataxia 1, Friedreich ataxia type 1
19 clinical trials for this condition and its sub-types, 1 tagged with Friedreich ataxia 1 itself.
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