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 |
| 5399432014 | 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 |
| 5399433016 | 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 |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Is a | Hereditary platelet function disorder (disorder) | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Is a | Digestive system hereditary disorder (disorder) | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Is a | Chronic digestive system disorder | false | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Is a | Gastrointestinal ulcer | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Is a | Recurrent disease | true | Inferred relationship | Some | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Clinical course | Recurrent | true | Inferred relationship | Some | 3 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Finding site | Gastrointestinal tract structure | true | Inferred relationship | Some | 2 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Associated morphology | Recurrent ulcer | false | Inferred relationship | Some | 2 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) | Associated morphology | Ulcer | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)
FHIR