Showing entry for Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation

General Disease Information
BXGD Id	BXGD024053
Disease Name	Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
Disease CUI Id	C4749281
MeSH Codes	C23   C10   F03   F01
Disease Class Name	Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
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