Disease #06642 (EIEE78 (Epileptic encephalopathy, early infantile, 78), OMIM:618557)

Official abbreviation EIEE78
Name Epileptic encephalopathy, early infantile, 78
OMIM ID 618557
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 GABRA2
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00414213 159194 - - M ? Turkey - - - - - EIEE78 Global developmental delay, Hypotonia GABRA2 GABRA2 1 1 Andreas Laner
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