Disease #05466 (EHLMRS (epilepsy, hearing loss, and mental retardation syndrome (EHLMRS)), OMIM:616577)

Official abbreviation EHLMRS
Name epilepsy, hearing loss, and mental retardation syndrome (EHLMRS)
OMIM ID 616577
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SPATA5
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2018-08-17 11:43:30 +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     
00404729 192779 - - F no Germany - - - - - EHLMRS Hearing Hypsarrhythmia, impairment, Global developmental delay, Seizure SPATA5 SPATA5 2 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.