Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
110621000077110 | anomalie congénitale du fibrinogène | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
351284017 | Congenital fibrinogen abnormality | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
382291000077117 | anomalie congénitale du fibrinogène (trouble) | fr | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Common French translation module (core metadata concept) |
622778010 | Congenital fibrinogen abnormality (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Hereditary factor I deficiency disease | est un(e) (attribut) | True | anomalie congénitale du fibrinogène | Inferred relationship | Some | |
Hypofibrinogenaemia | est un(e) (attribut) | False | anomalie congénitale du fibrinogène | Inferred relationship | Some | |
Hypodysfibrinogenaemia | est un(e) (attribut) | True | anomalie congénitale du fibrinogène | Inferred relationship | Some | |
Dysfibrinogenemia | est un(e) (attribut) | True | anomalie congénitale du fibrinogène | Inferred relationship | Some |
This concept is not in any reference sets