Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3303273015 | Glomuvenous malformation (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3303274014 | Glomuvenous malformation | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303275010 | Hereditary multiple glomangioma | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303276011 | Venous malformations with glomus cells | en | Synonym | Active | Case insensitive | SNOMED CT core |
3303277019 | Hereditary vascular malformations featuring the presence of small, multifocal bluish-purple venous lesions involving the skin. May be present at birth, and slowly expand during childhood. New small lesions appear with time. Often painful on palpation and cannot be completely emptied by compression. They are usually multifocal and are located mainly on the extremities, involving the skin and subcutis. Caused by mutations in the gene encoding glomulin and inherited in an autosomal dominant manner. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Problem/Diagnosis reference set