Phenotypes for disease #01362 (FHM1 (migraine, hemiplegic, familial, type 1), OMIM:141500)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000087182 passing right-sided hemisymptomatics with aphasia and headache, later on progressing loss of memory and disturbances of equilibrium; mother suffers from regular migraine attacks; twin brother shows peculiar nature, gait and speech - - Unknown - - - - - Birgit Neitzel 00110594
0000210719 - - - Familial, autosomal dominant 14y - - - - Pietro Palumbo 00239984
0000242700 one year old patient with tonic upward-looking - - Unknown 01y - - - - Andreas Laner 00324119
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