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DO Term : familial focal epilepsy with variable foci 3 [DOID:0081423] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A familial focal epilepsy with variable foci that has_material_basis_in heterozygous mutation in the NPRL3 gene on chromosome 16p13.
  • synonyms:
  • OMIM:617118,
  • 617118
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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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