Phenotypes for disease #02324 (arrhythmia, cardiac (arrhythmia, cardiac, ankyrin B-related), OMIM:600919)

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000271599 recurrent episodes of agitation and paleness accompanied by VT showed in ECG . Blood tests showed a mild increase in cardiac troponin I and myocardial enzymes, and normal electrolytes and glucose. Echocardiography showed normal heart structure and function. Brugada syndrome incessant ventricular tachycardias Familial, autosomal dominant 02y 00y07m ? recurrent episodes of agitation and paleness accompanied by VT showed in ECG - Chunli Wang 00376391
0000271659 recurrent VT episodes,ASD and PDA VT VT Familial, autosomal dominant <01y 01y - recurrent VT episodes - Chunli Wang 00376452
0000326855 see paperp; ..., dilated cardiomyopathy; sudden cardiac death; post-activity shortness of breath, palpitation, syncope without muscular strength involvement; ECG atrial fibrillation, paroxysmal ventricular tachycardia, frequent ventricular premature diffuse ventricular block dilated cardiomyopathy - Familial, autosomal dominant 31y - - - - Xuebin Ling 00436740
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.