Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 5136952018 | Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
| 5136953011 | Neonatal purpura fulminans due to homozygous protein C 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 |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Is a | Purpura fulminans | true | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Finding site | Blood vessel structure of skin (body structure) | false | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Course | Acute fulminating | false | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Associated morphology | Purpura | false | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Finding site | Structure of capillary blood vessel | false | Inferred relationship | Some | 1 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Finding site | Structure of skin region | false | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Finding site | Entire hematological system (body structure) | false | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Associated morphology | Necrosis | false | Inferred relationship | Some | 2 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Associated morphology | Thrombus (morphologic abnormality) | false | Inferred relationship | Some | 1 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Has definitional manifestation | Hemostatic system finding | false | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Clinical course | Acute fulminating | true | Inferred relationship | Some | 4 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Has definitional manifestation | Purpura | false | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Associated morphology | Thrombus (morphologic abnormality) | true | Inferred relationship | Some | 1 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Associated morphology | Necrosis | true | Inferred relationship | Some | 2 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Finding site | Structure of capillary blood vessel | true | Inferred relationship | Some | 1 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Is a | Homozygous protein C deficiency (disorder) | true | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Associated morphology | Purpura | true | Inferred relationship | Some | 3 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 3 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Interprets | Hemostatic function | true | Inferred relationship | Some | 5 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 5 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Some | ||
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Due to | Homozygous protein C deficiency (disorder) | true | Inferred relationship | Some | 6 | |
| Neonatal purpura fulminans due to homozygous protein C deficiency (disorder) | Is a | Purpura of skin and/or skin-associated mucous membrane co-occurrent and due to coagulation disorder (disorder) | true | Inferred relationship | Some |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR