Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2022. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 2788736011 | Hereditary antithrombin III deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 2791100010 | Hereditary antithrombin III deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Hereditary antithrombin III deficiency (disorder) | Is a | Hereditary thrombophilia (disorder) | true | Inferred relationship | Some | ||
| Hereditary antithrombin III deficiency (disorder) | Is a | Antithrombin III deficiency | true | Inferred relationship | Some | ||
| Hereditary antithrombin III deficiency (disorder) | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Hereditary antithrombin III deficiency (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | |
| Hereditary antithrombin III deficiency (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Hereditary antithrombin III deficiency (disorder) | Interprets | Plasma antithrombin III activity | true | Inferred relationship | Some | 2 | |
| Hereditary antithrombin III deficiency (disorder) | Has interpretation | Abnormally low (qualifier value) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR