Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
2983304019 | Long QT syndrome with syndactyly | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
2983535012 | Timothy syndrome type 1 (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
2983538014 | Timothy syndrome classic type | en | Synonym | Active | Case sensitive | SNOMED CT core |
2983544013 | Timothy syndrome type 1 | en | Synonym | Active | Case sensitive | SNOMED CT core |
3318416013 | Timothy syndrome is a multi-system disorder with characteristics of cardiac, hand, facial and neurodevelopmental features that include QT prolongation, webbed fingers and toes, flattened nasal bridge, low-set ears, small upper jaw, thin upper lip, and characteristic features of autism or autistic spectrum disorders. Timothy syndrome is caused by mutations in the CACNA1C gene. It is inherited as autosomal dominant trait. | 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