Phenotypes for disease #02864 (SQT3 (QT syndrome, short, type 3 (SQT-3)), OMIM:609622)

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     
0000154530 short QT syndrome, narrow and peaked T waves - - Familial, autosomal dominant - 5y 5y abnormal ECG - Ikuko Takeda 00206660
0000154566 paroxysmal AF, mild left ventricular dysfunction, short QT syndrome - - Isolated (sporadic) - 11y 8y Af - Ikuko Takeda 00206696
0000154574 shortened QT interval, paroxysmal AF, VF inducibility, mental retardation, abnormal proliferation of oesophageal blood vessels, epilepsy, Kawasaki disease - - - - 8y - - - Ikuko Takeda 00206704
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