autosomal recessive spinocerebellar ataxia 10

Term ID

DOID:0050999

Synonyms

• SCAR10

Definition

An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene. https://www.omim.org/entry/613728

References

• OMIM:613728

Ontology

Human Disease   ( DOID:0050999 )