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hereditary ataxia

Disease Summary
Associated Targets (225)
Tbio

168

Tchem

35

Tclin

13

Tdark

9


GARD Rare
Mondo Description An instance of an atactic disorder that is caused by an inherited genomic modification in an individual.
Disease Ontology Description A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements.
Mondo Term and Equivalent IDs
MONDO:0100309:  hereditary ataxia
GARD:0006614: 
GARD:0010748: 
ICD10:G11: 
MESH:C531684: 
Orphanet:183518: 
SCTID:763597000: