Phenotypes for disease #01185 (EA2 (ataxia, episodic, type 2), OMIM:108500)

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     
0000087186 episodic atxia - - Unknown - - - - - Birgit Neitzel 00110614
0000087190 episodic atxia - - Unknown - - - - - Birgit Neitzel 00110645
0000251168 (+) Ataxia,(+) Vertigo,(+) Abnormality of coordination - - Unknown 12y - - - - Andreas Laner 00332980
0000340669 Gait disturbance, Vertigo, Iron deficiency anemia, Ataxia, episodic, family history (father and brother) - - Familial, autosomal dominant 25y - - - - Andreas Laner 00452065
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