Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3302924012 | Deafness and oligodontia syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3302925013 | Deafness and oligodontia syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3302926014 | Rare syndrome with manifestation of sensorineural hearing loss and oligodontia/hypodontia. It has been described in two pairs of siblings and in one isolated case. Transmission appears to be autosomal recessive. | 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