Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module
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 | SNOMED CT core module |
| 4636406016 | PLA2G4A (phospholipase A2 group IVA) related platelet dysfunction | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4636407013 | PLA2G4A-related platelet dysfunction | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 4636408015 | Platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4636409011 | Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Is a | Hereditary platelet function disorder | true | Inferred relationship | Existential restriction modifier | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Is a | Digestive system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Interprets | Hemostatic function | true | Inferred relationship | Existential restriction modifier | 1 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Has interpretation | Abnormal | true | Inferred relationship | Existential restriction modifier | 1 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Is a | Chronic digestive system disorder | false | Inferred relationship | Existential restriction modifier | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Is a | Gastrointestinal ulcer | true | Inferred relationship | Existential restriction modifier | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Is a | Recurrent disease | true | Inferred relationship | Existential restriction modifier | ||
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Clinical course | Recurrent | true | Inferred relationship | Existential restriction modifier | 3 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Finding site | Gastrointestinal tract structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Associated morphology | Recurrent ulcer | false | Inferred relationship | Existential restriction modifier | 2 | |
| Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder | Associated morphology | Ulcer | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR