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Disease association ontology term - MONDO:0012664 - spastic ataxia 3

Term summary

ID
MONDO:0012664
Name
spastic ataxia 3
Ontology or CV name
Disease association
Definition
Any autosomal recessive spastic ataxia in which the cause of the disease is a mutation in the MARS2 gene.

Parents

Annotation

Disease association

MONDO:0012664 - spastic ataxia 3

References:

Genes: