Disease #05435 (DEE92;IECEE2 (encephalopathy, developmental and epileptic, type92 (IECEE2)), OMIM:617829)

Official abbreviation DEE92;IECEE2
Name encephalopathy, developmental and epileptic, type92 (IECEE2)
OMIM ID 617829
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 GABRB2
Associated tissues -
Disease features autosomal dominant
Remarks -
Date created 2018-06-01 14:38:04 +02:00 (CEST)
Date last edited 2023-10-23 12:25:49 +02:00 (CEST)


Individuals

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00466207 340374 - - F no Iraq Kurdisch - - - - DEE92;IECEE2 Generalized-onset seizure, Febrile seizure outside the age of 3 months to 6 years, Neurodevelopmental delay GABRB2 GABRB2 1 1 Andreas Laner
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