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MIRAGE
congenital bile acid synthesis defect 2
Summary
- Synonym
-
- CBAS2
- cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency
- Definition
- A congenital bile acid synthesis defect characterized by rapid progession of severe cholestatic liver disease, decreased levels of chenodeoxycholic acid and cholic acid in the serum and urine, and malabsorption of fat and fat-soluble vitamins that has_material_basis_in homozygous or compound heterozygous mutation in the AKR1D1 gene on chromosome 7q33.
- Super Class
- congenital bile acid synthesis defect
External Links
- Disease Ontology
- DOID:0111069
- Mondo Disease Ontology
- MeSH
- UMLS
- ORDO
- GARD
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003256 | Abnormality of the coagulation cascade |
| HP:0000107 | Renal cyst |
| HP:0001978 | Extramedullary hematopoiesis |
| HP:0003645 | Prolonged partial thromboplastin time |
| HP:0001399 | Hepatic failure |
| HP:0011040 | Abnormal intrahepatic bile duct morphology |
| HP:0001508 | Failure to thrive |
| HP:0002240 | Hepatomegaly |
| HP:0100513 | Decreased circulating vitamin E concentration |
| HP:0002630 | Fat malabsorption |
