Disease #00009 (ABCB1 (Epilepsy syndrome), OMIM:171050)

Official abbreviation ABCB1
Name Epilepsy syndrome
OMIM ID 171050
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ABCB1
Associated tissues hippocampus
Disease features -
Remarks -

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