Showing entry for Hepatic methionine adenosyltransferase deficiency

General Disease Information
BXGD Id	BXGD006012
Disease Name	Hepatic methionine adenosyltransferase deficiency
Disease CUI Id	C0268621
MeSH Codes	C16   C18
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; 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