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DO Term : autosomal dominant nocturnal frontal lobe epilepsy 3 [DOID:0060684] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  An autosomal dominant nocturnal frontal lobe epilepsy that has_material_basis_in heterozygous mutation in the CHRNB2 gene on chromosome 1q21.
  • synonyms:
  • OMIM:605375,
  • nocturnal frontal lobe epilepsy 3,
  • ENFL3,
  • 605375
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Disease

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Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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