Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3643231015 | Lichtenstein syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
| 3643232010 | Lichtenstein syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
| 3643233017 | Syndrome with characteristics of frequent infections associated with osteoporosis, a tendency for fractures and osseous anomalies. It has been described in two monozygotic twin brothers. Transmission is autosomal recessive. | en | Definition | Active | Case sensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Lichtenstein syndrome | Pathological process | Abnormal immune process | true | Inferred relationship | Some | 2 | |
| Lichtenstein syndrome | Is a | Congenital immunodeficiency disease | true | Inferred relationship | Some | ||
| Lichtenstein syndrome | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Some | ||
| Lichtenstein syndrome | Is a | Phagocytic cell dysfunction | true | Inferred relationship | Some | ||
| Lichtenstein syndrome | Is a | Hereditary disorder of immune system | true | Inferred relationship | Some | ||
| Lichtenstein syndrome | Is a | Disorder of immune structure | true | Inferred relationship | Some | ||
| Lichtenstein syndrome | Finding site | Structure of immune system | true | Inferred relationship | Some | 1 | |
| Lichtenstein syndrome | Occurrence | Congenital | 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