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Disease association ontology term - MONDO:0100340 - Friedreich ataxia 1

Term summary

ID
MONDO:0100340
Name
Friedreich ataxia 1
Ontology or CV name
Disease association
Definition
Any Friedreich ataxia in which the cause of the disease is a mutation in the FXN gene.

Parents

Annotation

Disease association

MONDO:0100340 - Friedreich ataxia 1

References:

Genes: