Disease #05903 (EPM11 (epilepsy, progressive myoclonic, type 11 (EPM11)), OMIM:608873)

Official abbreviation EPM11
Name epilepsy, progressive myoclonic, type 11 (EPM11)
OMIM ID 608873
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 SEMA6B
Associated tissues -
Disease features -
Remarks -
Date created 2021-03-03 09:35:15 +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     
00381542 183752 - - M ? Turkey - - - - - EPM11 Intellectual disability, Seizure, Generalized non-motor (absence) seizure, Intellectual disability, borderline, Stuttering, Enuresis SEMA6B SEMA6B 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.