Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303974016 | Non-Wilsonian hepatic copper toxicosis of infancy and childhood | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3304658017 | Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3304659013 | Idiopathic copper associated cirrhosis of liver | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3303976019 | A rare copper-overload liver disease with rapidly progressive liver cirrhosis from the first few years of life leading to hepatic insufficiency. Specific pathological aspects; pericellular fibrosis, inflammatory infiltration, hepatocyte necrosis, absence of steatosis, poor regeneration and histochemical copper staining. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | est un(e) (attribut) | Cryptogenic cirrhosis | true | Inferred relationship | Some | ||
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | est un(e) (attribut) | Disorder of liver due to disorder of mineral metabolism (disorder) | true | Inferred relationship | Some | ||
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | est un(e) (attribut) | maladie idiopathique | false | Inferred relationship | Some | ||
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | localisation d'une constatation (attribut) | foie | true | Inferred relationship | Some | 2 | |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | Due to | Disorder of copper metabolism | true | Inferred relationship | Some | 3 | |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | est un(e) (attribut) | Cirrhosis of liver | false | Inferred relationship | Some | ||
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | survenue (attribut) | Infancy (qualifier value) | true | Inferred relationship | Some | 4 | |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | survenue (attribut) | enfance | true | Inferred relationship | Some | 5 | |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | morphologie associée (attribut) | Nodular regeneration | false | Inferred relationship | Some | 4 | |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | morphologie associée (attribut) | Fibrosis | false | Inferred relationship | Some | 4 | |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | localisation d'une constatation (attribut) | foie | false | Inferred relationship | Some | 4 | |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | évolution clinique (attribut) | progressif | true | Inferred relationship | Some | 6 | |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | localisation d'une constatation (attribut) | foie | true | Inferred relationship | Some | 1 | |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | morphologie associée (attribut) | Chronic fibrosis (morphologic abnormality) | true | Inferred relationship | Some | 2 | |
Non-Wilsonian hepatic copper toxicosis of infancy and childhood (disorder) | morphologie associée (attribut) | Nodular regeneration | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets