Showing entry for Primary lactose intolerance

General Disease Information
BXGD Id	BXGD007544
Disease Name	Primary lactose intolerance
Disease CUI Id	C0342759
MeSH Codes	C16   C06   C18
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; 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