Disease #06281 (EIEE79 (Epileptic encephalopathy, early infantile, 79), OMIM:618559)

Official abbreviation EIEE79
Name Epileptic encephalopathy, early infantile, 79
OMIM ID 618559
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GABRA5
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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