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spastic ataxia 3

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any autosomal recessive spastic ataxia in which the cause of the disease is a mutation in the MARS2 gene.
Uniprot Description A neurologic disorder characterized by cerebellar ataxia, ataxic gait, spasticity, and hyperreflexia. Other variable features include dysarthria, dysmetria, mild cognitive impairment, urinary urgency and dystonic positioning.
Mondo Term and Equivalent IDs
MONDO:0012664:  spastic ataxia 3
MESH:C566956: 
Orphanet:314603: 
UMLS:C1969645: 
UMLS:CN230089: