Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3759333015 | Hypotrichosis and deafness syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3759334014 | Hypotrichosis and deafness syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3759335010 | A syndromic genetic deafness with characteristics of erythrokeratoderma, hypotrichosis, nail dystrophy and sensorineural hearing loss. Erythema, recurrent skin infections and mucositis have also been 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