Showing entry for Epilepsy, Benign Neonatal, 3

General Disease Information
BXGD Id	BXGD014514
Disease Name	Epilepsy, Benign Neonatal, 3
Disease CUI Id	C1842382
MeSH Codes	C16   C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations