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DO Term : idiopathic generalized epilepsy 11 [DOID:0111312] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An idiopathic generalized epilepsy that has_material_basis_in heterozygous mutation in the CLCN2 on chromosome 3q27.1.

synonyms:
607628,
EIG11,
OMIM:607628

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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