Showing entry for Autosomal dominant hyperinsulinism due to Kir6.2 deficiency

General Disease Information
BXGD Id	BXGD022343
Disease Name	Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
Disease CUI Id	C4274081
MeSH Codes	C18
Disease Class Name	Nutritional and Metabolic 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