congenital bile acid synthesis defect 4

Summary
Synonym
  • CBAS4
  • intrahepatic cholestasis with defective conversion of trihydroxycoprostanic acid to cholic acid
  • trihydroxycoprostanic acid in bile
Definition
A congenital bile acid synthesis defect characterized by intrahepatic cholestasis, malabsorption of fat and fat-soluble vitamins, decreased serum cholesterol, and increased levels of THCA in bile, serum and urine that has_material_basis_in homozygous mutation in the AMACR gene on chromosome 5p13.
Super Class
congenital bile acid synthesis defect
Disease Ontology
DOID:0111068
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
23600 AMACR alpha-methylacyl-CoA racemase
The Human Phenotype Ontology
Displaying entries 21 - 30 of 39 in total
HPO ID HPO Term
HP:0005978 Type II diabetes mellitus
HP:0007141 Sensorimotor neuropathy
HP:0011892 Decreased circulating vitamin K concentration
HP:0012379 Abnormal circulating enzyme concentration or activity
HP:0100753 Schizophrenia
HP:0200084 Giant cell hepatitis
HP:0000007 Autosomal recessive inheritance
HP:0001399 Hepatic failure
HP:0001406 Intrahepatic cholestasis
HP:0001508 Failure to thrive
Displaying 1 entry
Gene ID Gene Symbol Description
23600 AMACR alpha-methylacyl-CoA racemase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024