Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1770542018 | Endogenous non-melanin pigmentation (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
| 1781732019 | Endogenous non-melanin pigmentation | en | Synonym | Active | Case insensitive | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Endogenous non-melanin pigmentation | Is a | Disorder of skin colour | true | Inferred relationship | Some | ||
| Endogenous non-melanin pigmentation | Finding site | Skin structure | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
| Skin pigmentation due to haemosiderosis | Is a | True | Endogenous non-melanin pigmentation | Inferred relationship | Some | |
| Ochronosis due to alkaptonuria | Is a | False | Endogenous non-melanin pigmentation | Inferred relationship | Some | |
| Bronze baby | Is a | True | Endogenous non-melanin pigmentation | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
FHIR