Disease #03075 (ECA6 (epilepsy, childhood absence, type 6 (ECA-6)), OMIM:611942)

Official abbreviation ECA6
Name epilepsy, childhood absence, type 6 (ECA-6)
OMIM ID 611942
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CACNA1H
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

1 entry on 1 page. Showing entry 1.
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     
00455167 306547 - - F no Germany - - - - - ECA6 EEG abnormality, Febrile seizure (within the age range of 3 months to 6 years), Complex febrile seizure CACNA1H CACNA1H 1 1 Andreas Laner
Legend   How to query  


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