Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3316420016 | Congenital bile acid synthesis defect type 3 (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3316421017 | Congenital bile acid synthesis defect type 3 | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3316422012 | Oxysterol 7-alpha hydroxylase deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3316423019 | A severe anomaly of bile acid synthesis with manifestation of severe neonatal cholestatic liver disease. To date, only 2 cases of this disorder have been reported. Caused by mutations in the 7-alpha hydroxylase gene (CYP7B1, 8q21.3). The deficiency in oxysterol 7-alpha-hydroxylation leads to the accumulation of hepatotoxic unsaturated monohydroxy bile acids. The mode of transmission is presumed to be autosomal recessive. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
972701000172111 | déficit congénital de synthèse des acides biliaires type 3 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
992381000172111 | DSAB3 - déficit congénital de synthèse des acides biliaires type 3 | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
880201000172119 | congenitaal galzuursynthesedefect type 3 | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | Belgian module (core metadata concept) |
942011000172110 | BASD3 - bile acid synthesis defect type 3 | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | Belgian module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital bile acid synthesis defect type 3 (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Congenital bile acid synthesis defect type 3 (disorder) | Is a | Synthetic defect of bile acids (disorder) | true | Inferred relationship | Some | ||
Congenital bile acid synthesis defect type 3 (disorder) | Is a | Digestive system hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Congenital bile acid synthesis defect type 3 (disorder) | Finding site | Liver structure | true | Inferred relationship | Some | 1 | |
Congenital bile acid synthesis defect type 3 (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets