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Disease association ontology term - MONDO:0014934 - spinocerebellar ataxia, autosomal recessive 24

Term summary

ID
MONDO:0014934
Name
spinocerebellar ataxia, autosomal recessive 24
Ontology or CV name
Disease association
Definition
Any autosomal recessive cerebellar ataxia in which the cause of the disease is a mutation in the UBA5 gene.

Parents

Annotation

Disease association

MONDO:0014934 - spinocerebellar ataxia, autosomal recessive 24

References:

Genes: