Showing entry for EPILEPSY, BENIGN NEONATAL, 2

General Disease Information
BXGD Id	BXGD015294
Disease Name	EPILEPSY, BENIGN NEONATAL, 2
Disease CUI Id	C1852581
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	DOID:7
Disease Ontology Class Name	disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations