Showing entry for Glycogen Storage Disease XII



                               
General Disease Information
BXGD IdBXGD006299
Disease NameGlycogen Storage Disease XII
Disease CUI IdC0272066
MeSH Codes C16   C18  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id   
Disease Ontology Class Name
Disorder Network disorder-protein-compound-food associations