Showing entry for Hyperinsulinemic hypoglycemia, familial, 2



                               
General Disease Information
BXGD IdBXGD018071
Disease NameHyperinsulinemic hypoglycemia, familial, 2
Disease CUI IdC2931833
MeSH Codes C16   C06   C18  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:0014667   DOID:630  
Disease Ontology Class Namedisease of metabolism; genetic disease
Disorder Network disorder-protein-compound-food associations