Phenotypes for disease #02542 (SCA14 (ataxia, spinocerebellar, type 14 (SCA-14)), OMIM:605361)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000053283 - - - Familial, autosomal dominant - - - - - Claire Guissart 00073124
0000053284 - - - Familial, autosomal dominant - - - - - Claire Guissart 00073123
0000084358 - - - Familial, autosomal dominant 73y - - - - Friederike Hein 00106553
0000283590 Ataxia, Cerebellar atrophy, Spastic paraplegia, Optic neuropathy, Dysarthria, Difficulty in tongue movements, Hyperreflexia; Son (untested) with similar symptoms - - Familial, autosomal dominant - 30y - - - Andreas Laner 00390050
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