Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 66901019 | Familial C3B inhibitor deficiency syndrome | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
| 776173013 | Familial C3B inhibitor deficiency syndrome (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial C3B inhibitor deficiency syndrome | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 2 | |
| Familial C3B inhibitor deficiency syndrome | Is a | Complement regulatory factor defect | true | Inferred relationship | Some | ||
| Familial C3B inhibitor deficiency syndrome | Is a | Hereditary disorder of immune system | true | Inferred relationship | Some | ||
| Familial C3B inhibitor deficiency syndrome | Is a | Familial disease | true | Inferred relationship | Some | ||
| Familial C3B inhibitor deficiency syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Familial C3B inhibitor deficiency syndrome | Has definitional manifestation | Immune system finding | false | Inferred relationship | Some | ||
| Familial C3B inhibitor deficiency syndrome | Finding site | Structure of immune system | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR