Status: current. Date: 31-Jul 2022
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5084123019 | Idiopathic ductopenia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5084124013 | IAD - idiopathic adult ductopenia | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5084125014 | Idiopathic ductopenia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5084126010 | Idiopathic adult ductopenia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5084127018 | A rare biliary tract disease with characteristics of loss of interlobular bile ducts resulting in chronic cholestasis, without any known cause. Loss of less than 50% of interlobular bile ducts is associated with a mild disease course, while loss of the majority of ducts results in a severe form, potentially leading to cirrhosis and liver failure. Patients typically present as young or middle-aged adults with episodic jaundice, pruritus and elevated liver enzymes. | en | Definition | Inactive | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400219013 | A rare biliary tract disease characterized by loss of interlobular bile ducts resulting in chronic cholestasis, without any known cause. Loss of less than 50% of interlobular bile ducts is associated with a mild disease course, while loss of the majority of ducts results in a severe form, potentially leading to cirrhosis and liver failure. Patients typically present as young or middle-aged adults with episodic jaundice, pruritus, and elevated liver enzymes. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 5400220019 | A rare biliary tract disease characterised by loss of interlobular bile ducts resulting in chronic cholestasis, without any known cause. Loss of less than 50% of interlobular bile ducts is associated with a mild disease course, while loss of the majority of ducts results in a severe form, potentially leading to cirrhosis and liver failure. Patients typically present as young or middle-aged adults with episodic jaundice, pruritus, and elevated liver enzymes. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Idiopathic ductopenia (disorder) | Is a | Chronic liver disease | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Idiopathic ductopenia (disorder) | Is a | Idiopathic disease | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | ||
| Idiopathic ductopenia (disorder) | Occurrence | Adulthood | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| Idiopathic ductopenia (disorder) | Finding site | Structure of interlobular bile duct | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 1 | |
| Idiopathic ductopenia (disorder) | Clinical course | Chronic | true | Congenital syphilitic hepatomegaly | Congenital syphilitic hepatomegaly | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR