Status: current, Defined. Date: 31-Jan 2020. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
1771730019 | Hereditary hypermelanosis (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
1782813016 | Hereditary hypermelanosis | en | Synonym | Active | Case insensitive | SNOMED CT core |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set
Description inactivation indicator reference set