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DO Term : early-onset epilepsy 2 [DOID:0070471] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An epilepsy characterized by neonatal to childhood onset of generalized tonic-clonic seizures that has_material_basis_in heterozygous mutation in the SETD1A gene on chromosome 16p11.2.

synonyms:
OMIM:618832,
618832,
EPEO2

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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