Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module | 
| 158737014 | Hereditary hypoplasminogenemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | 
| 512324012 | Hereditary hypoplasminogenaemia | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | 
| 840080012 | Hereditary hypoplasminogenemia (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core | 
| 1944561000052119 | ärftlig plasminogenbrist | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) | 
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values | 
| Hereditary hypoplasminogenemia | Is a | Hypoplasminogenaemia | true | Inferred relationship | Some | ||
| Hereditary hypoplasminogenemia | Is a | Hereditary disorder of hematologic system | false | Inferred relationship | Some | ||
| Hereditary hypoplasminogenemia | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Hereditary hypoplasminogenemia | Is a | Hereditary disorder by system | false | Inferred relationship | Some | ||
| Hereditary hypoplasminogenemia | Finding site | Body system structure | false | Inferred relationship | Some | ||
| Hereditary hypoplasminogenemia | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Hereditary hypoplasminogenemia | Is a | Hereditary disease | true | Inferred relationship | Some | ||
| Hereditary hypoplasminogenemia | Interprets | Hemostatic function | true | Inferred relationship | Some | 1 | |
| Hereditary hypoplasminogenemia | Has interpretation | Abnormal | true | Inferred relationship | Some | 1 | 
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Autosomal dominant deficiency of plasminogen | Is a | True | Hereditary hypoplasminogenemia | Inferred relationship | Some | 
This concept is not in any reference sets