SETX, senataxin, 23064

N. diseases: 133; N. variants: 39
Disease: Movement Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation group CLINVAR Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. 19696032 2009
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation group CLINVAR Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients. 19696032 2009
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation group CLINVAR Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy. 15732101 2005
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation group CLINVAR Mutations in senataxin responsible for Quebec cluster of ataxia with neuropathy. 15732101 2005
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation group CLINVAR Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. 14770181 2004
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 CausalMutation group CLINVAR DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). 15106121 2004
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation group CLINVAR Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. 14770181 2004
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		0.100 GeneticVariation group CLINVAR DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). 15106121 2004