Disease #00122 (LQT1 (Long QT Syndrome), OMIM:192500)

Official abbreviation LQT1
Name Long QT Syndrome
OMIM ID 192500
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene KCNQ1
Associated tissues -
Disease features -
Remarks -


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

Reference     

Gender     

Geographic origin     

Ethnic origin     

Population     

Remarks     

Microattribution     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00000648 A R Wong et al.(2019) M Kelantan Malay - - - LQT1 - KCNQ1 KCNQ1 1 1 Nur Aisyah Athirah
Legend   How to query