Disease #01889 (FESD (epilepsy, focal, with speech disorder with/without mental retardation (FESD)), OMIM:245570)

Official abbreviation FESD
Name epilepsy, focal, with speech disorder with/without mental retardation (FESD)
OMIM ID 245570
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene GRIN2A
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

2 entries on 1 page. Showing entries 1 - 2.
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00074422 - - - M no Spain - - - - - FESD, ID - GRIN2A GRIN2A 1 1 NeuroMeGen
00444352 266427 - - M no Germany - - - - - FESD Seizure, Neurodevelopmental delay GRIN2A GRIN2A 1 1 Andreas Laner
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