Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3704772013 | Hypertrichosis cubiti (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3704773015 | Hypertrichosis cubiti | en | Synonym | Active | Case insensitive | SNOMED CT core |
3704774014 | Hairy elbows syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3704775010 | MacDermot Patton Williams syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3704776011 | A rare hair anomaly characterised by symmetrical, congenital or early-onset, bilateral hypertrichosis localised on the extensor surfaces of the upper extremities (especially the elbows). Short stature, or other abnormalities, such as developmental delay, facial anomalies and intellectual disability, may or may not be associated. | en | Definition | Active | Case sensitive | SNOMED CT core |
3704777019 | A rare hair anomaly characterized by symmetrical, congenital or early-onset, bilateral hypertrichosis localized on the extensor surfaces of the upper extremities (especially the elbows). Short stature, or other abnormalities, such as developmental delay, facial anomalies and intellectual disability, may or may not be associated. | 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
Problem/Diagnosis reference set