Disease #07065 (DEE99 (encephalopathy, developmental and epileptic, type 99), OMIM:619606)

Official abbreviation DEE99
Name encephalopathy, developmental and epileptic, type 99
OMIM ID 619606
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ATP1A3
Associated tissues -
Disease features -
Remarks -
Date created 2024-01-26 15:23:29 +01:00 (CET)
Date last edited N/A


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     
00470629 354113 - - F no Germany - - - - - DEE99 Febrile seizure (within the age range of 3 months to 6 years), Febrile seizure outside the age of 3 months to 6 years ATP1A3 ATP1A3 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.