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hereditary ataxia

Disease Summary
Associated Targets (214)
Tbio

160

Tchem

30

Tclin

13

Tdark

11


Explore Associated Targets
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: 
GWAS Targets (0)
No GWAS traits found
Disease Hierarchy
Target Novelty (Tin-x)