Phenotypes for disease #00208 (GSD (Gerstmann-Straussler disease (GSD)), OMIM:137440)

14 entries on 1 page. Showing entries 1 - 14.
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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     
0000002904 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00004164
0000002905 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00004165
0000002913 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00004173
0000002915 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00004175
0000002916 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00004176
0000002917 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00004177
0000002918 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00004178
0000002919 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00004179
0000002926 - - - Isolated (sporadic) - - - - - Johan den Dunnen 00004186
0000002942 - - - Unknown - - - - - Johan den Dunnen 00004202
0000002943 - - - Unknown - - - - - Johan den Dunnen 00004203
0000002947 - - - Unknown - - - - - Johan den Dunnen 00004207
0000002952 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00004212
0000016203 typical history of Gerstmann-Straussler syndrome incl. progressive cerebellar ataxia, late cognitive decline, 5y disease duration - - Familial, autosomal dominant 56y - - - - Johan den Dunnen 00017850
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