Showing entry for Disorder of sulfur-bearing amino acid metabolism



                               
General Disease Information
BXGD IdBXGD006008
Disease NameDisorder of sulfur-bearing amino acid metabolism
Disease CUI IdC0268613
MeSH Codes C23   C16   C18  
Disease Class NamePathological Conditions, Signs and Symptoms; Congenital, 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 DOID:0014667   DOID:630  
Disease Ontology Class Namedisease of metabolism; genetic disease
Disorder Network disorder-protein-compound-food associations