Disease #04538 (EIEE26 (encephalopathy, epileptic, early infantile, type 26 (EIEE-26)), OMIM:616056)

Official abbreviation EIEE26
Name encephalopathy, epileptic, early infantile, type 26 (EIEE-26)
OMIM ID 616056
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 2
Associated with 1 gene KCNB1
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

4 entries on 1 page. Showing entries 1 - 4.
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00391853 213P - - F no Spain - - - - - EIEE26 - - KCNB1 1 1 Alejandro Brea-Fernández
00401307 103P - - F no Spain - - - - - EIEE26, ID - - KCNB1 1 1 Alejandro Brea-Fernández
00436170 268773 - - F no Germany - - - - - EIEE26 Generalized-onset seizure, Neurodevelopmental delay KCNB1 KCNB1 1 1 Andreas Laner
00466204 340404 - - M no Germany - - - - - EIEE26 Neurodevelopmental delay, Expressive language delay, Status epilepticus, EEG abnormality KCNB1 KCNB1 1 1 Andreas Laner
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