Disease #02324 (arrhythmia, cardiac (arrhythmia, cardiac, ankyrin B-related), OMIM:600919)

Official abbreviation arrhythmia, cardiac
Name arrhythmia, cardiac, ankyrin B-related
OMIM ID 600919
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ANK2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-06-22 13:54:14 +02:00 (CEST)


Individuals

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

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00376391 - - - M no China Asian - - - - arrhythmia, cardiac 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. SCN5A SCN5A 1 1 Chunli Wang
00376452 - - - M no China asian - - - metoprolol arrhythmia, cardiac recurrent VT episodes,ASD and PDA SCN5A SCN5A 2 1 Chunli Wang
00436740 patient Ling 2023, submitted - M - China - - - - - arrhythmia, cardiac 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 LMNA LMNA 1 1 Xuebin Ling
Legend   How to query  


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