Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3330477018 | Oro-facial digital syndrome type 5 (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3330480017 | Oro-facial digital syndrome type 5 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3330708014 | Orofaciodigital syndrome type 5 | en | Synonym | Active | Case insensitive | SNOMED CT core |
3330709018 | Orofaciodigital syndrome Thurston type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3330710011 | Thurston syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3330711010 | Syndrome with characteristics of median cleft of upper lip, postaxial polydactyly of hands and feet and oral manifestations (duplicated frenulum). Less than 20 patients (predominantly of Indian origin) have been reported so far. Autosomal recessive inheritance has been suggested, but the causative gene has not yet been identified. | 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