Phenotypes for disease #00369 (DYT1 (dystonia, torsion, early onset, type 1 (DYT-1)), OMIM:128100)

5 entries on 1 page. Showing entries 1 - 5.
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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     
0000015016 highly variable phenotype, reduced penetrance - - Familial, autosomal dominant - - - - - Johan den Dunnen 00016414
0000015017 see paper - - Isolated (sporadic) - - - - - Johan den Dunnen 00016415
0000015018 see paper - - Isolated (sporadic) - - - - - Johan den Dunnen 00016417
0000015019 see paper - - Familial, autosomal dominant - - - - - Johan den Dunnen 00016418
0000015020 see paper, late-onset focal torsion dystonia - - Isolated (sporadic) - - - - - Johan den Dunnen 00016420
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