Ontological Term Details

Compound
FDB022137 (Coprocholic acid)
Term
Congenital Bile Acid Synthesis Defect Type III
Definition
the synthesis of primary bile acids from cholesterol occurs via two pathways: the classic neutral pathway involving cholesterol 7-alpha-hydroxylase (cyp7a1), and the acidic pathway involving a distinct microsomal oxysterol 7-alpha-hydroxylase (cyp7b1). cbasiii is characterized by accumulation of bile acids in the urine.
Parent Term
Biochemical pathway
Parent Definition
A linked series of chemical reactions that occur in a defined order within or between organism cells, and lead to a known function or end product.
Other Compounds Mapped to 'Congenital Bile Acid Synthesis Defect Type III'
  • FDB000484 (Glycine)
  • FDB031054 (NADP+)
  • FDB031084 (palmitate)
  • FDB021909 (NADPH)
  • FDB003191 (Taurine)
  • FDB022087 (Chenodeoxycholic acid)
  • FDB030683 (ATP)
  • FDB030724 (cholate)
  • FDB022152 (Deoxycholic acid glycine conjugate)
  • FDB022157 (Chenodeoxycholic acid glycine conjugate)
  • References