Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4636405017 | Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4636406016 | PLA2G4A (phospholipase A2 group IVA) related platelet dysfunction | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4636407013 | PLA2G4A-related platelet dysfunction | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4636408015 | Platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4636409011 | Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 4636410018 | A rare genetic haematologic and intestinal disease characterised by childhood onset of bleeding tendency with epistaxis, gum bleeding, gastrointestinal bleeding, haematuria and menorrhagia due to impaired platelet aggregation and secretion, as well as recurrent gastrointestinal ulcer. Mildly reduced levels of coagulation factor XI have been reported in addition. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 4636411019 | A rare genetic hematologic and intestinal disease characterized by childhood onset of bleeding tendency with epistaxis, gum bleeding, gastrointestinal bleeding, hematuria and menorrhagia due to impaired platelet aggregation and secretion, as well as recurrent gastrointestinal ulcer. Mildly reduced levels of coagulation factor XI have been reported in addition. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | est un(e) (attribut) | Hereditary platelet function disorder | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | est un(e) (attribut) | Digestive system hereditary disorder | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | est un(e) (attribut) | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | interprète (attribut) | Hemostatic function (observable entity) | true | Inferred relationship | Some | 1 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | a pour interprétation (attribut) | anormal | true | Inferred relationship | Some | 1 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | est un(e) (attribut) | affection chronique de l'appareil digestif | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | est un(e) (attribut) | ulcère gastro-intestinal | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | est un(e) (attribut) | affection récidivante | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | évolution clinique (attribut) | récurrent | true | Inferred relationship | Some | 3 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | localisation d'une constatation (attribut) | structure du tractus gastro-intestinal | true | Inferred relationship | Some | 2 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | morphologie associée (attribut) | Recurrent ulcer | false | Inferred relationship | Some | 2 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | morphologie associée (attribut) | ulcère (anomalie morphologique) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR