Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 18557013 | Insulin receptor defect | en | Synonym | Active | Case insensitive | SNOMED CT core |
| 584573013 | Insulin receptor defect (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Insulin receptor defect | Is a | Disorder of endocrine receptor | true | Inferred relationship | Some | ||
| Insulin receptor defect | Finding site | Structure of endocrine system | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Extreme insulin resistance with acanthosis nigricans, hirsutism AND abnormal insulin receptors | Is a | True | Insulin receptor defect | Inferred relationship | Some | |
| Diabetes mellitus associated with receptor abnormality | Associated with | True | Insulin receptor defect | Inferred relationship | Some | 1 |
| Hereditary benign acanthosis nigricans with insulin resistance | Is a | True | Insulin receptor defect | Inferred relationship | Some | |
| Acanthosis nigricans and insulin resistance with muscle cramp and acral enlargement syndrome | Is a | True | Insulin receptor defect | Inferred relationship | Some | |
| Hyperinsulinism due to insulin receptor deficiency | Due to | True | Insulin receptor defect | Inferred relationship | Some | 2 |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR