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DO Term : autosomal dominant nocturnal frontal lobe epilepsy 5 [DOID:0060686] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the KCNT1 gene on chromosome 9q34.

synonyms:
nocturnal frontal lobe epilepsy 5,
OMIM:615005,
ENFL5,
615005

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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