Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3727915012 | Neonatal antiphospholipid syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3727916013 | Neonatal antiphospholipid syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3727917016 | Neonatal Hughes syndrome | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 3727918014 | Neonatal antiphospholipid antibody syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3727919018 | A rare secondary neonatal autoimmune disease with characteristics of single or recurrent episodes of venous, arterial or mixed thrombosis in a neonate whose mother does not have antiphospholipid syndrome manifestations. Patients present positive antiphospholipid antibodies and may have additional abnormalities associated (for example cardiac valve disease, livedo reticularis, thrombocytopenia, nephropathy, neurological manifestations). | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 952871000172111 | APS (antiphospholipides) néonatal | fr | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| 965001000172112 | syndrome des antiphospholipides néonatal | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Neonatal antiphospholipid syndrome (disorder) | Is a | Antiphospholipid syndrome | true | Inferred relationship | Some | ||
| Neonatal antiphospholipid syndrome (disorder) | Is a | Acquired thrombophilia (disorder) | false | Inferred relationship | Some | ||
| Neonatal antiphospholipid syndrome (disorder) | Occurrence | Neonatal | true | Inferred relationship | Some | 1 | |
| Neonatal antiphospholipid syndrome (disorder) | Pathological process (attribute) | Autoimmune process | true | Inferred relationship | Some | 1 | |
| Neonatal antiphospholipid syndrome (disorder) | Is a | Neonatal disorder | true | Inferred relationship | Some | ||
| Neonatal antiphospholipid syndrome (disorder) | Interprets | Hemostatic function | true | Inferred relationship | Some | 2 | |
| Neonatal antiphospholipid syndrome (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 2 | |
| Neonatal antiphospholipid syndrome (disorder) | Causative agent | Anti-phospholipid antibody | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR