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 |
3307409016 | Congenital alpha-2-antiplasmin deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3307410014 | Congenital alpha-2-antiplasmin deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3307411013 | Congenital alpha2-antiplasmin deficiency | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3307412018 | A rare hemorrhagic disorder caused by congenital deficiency of alpha2 antiplasmin, leading to dysregulated fibrinolysis and is characterized by a hemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes. Inherited in an autosomal recessive manner. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3307413011 | A rare haemorrhagic disorder caused by congenital deficiency of alpha2 antiplasmin, leading to dysregulated fibrinolysis and is characterised by a haemorrhagic tendency presenting from childhood with prolonged bleeding and ecchymoses following minor trauma and spontaneous bleeding episodes. Inherited in an autosomal recessive manner. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital alpha-2-antiplasmin deficiency (disorder) | a pour interprétation (attribut) | anormal | true | Inferred relationship | Some | 2 | |
Congenital alpha-2-antiplasmin deficiency (disorder) | interprète (attribut) | Hemostatic function (observable entity) | true | Inferred relationship | Some | 2 | |
Congenital alpha-2-antiplasmin deficiency (disorder) | est un(e) (attribut) | Congenital disease | true | Inferred relationship | Some | ||
Congenital alpha-2-antiplasmin deficiency (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
Congenital alpha-2-antiplasmin deficiency (disorder) | est un(e) (attribut) | Alpha-2-antiplasmin deficiency | true | Inferred relationship | Some | ||
Congenital alpha-2-antiplasmin deficiency (disorder) | survenue (attribut) | congénital | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets