Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3321532017 | Cardiomyopathy and renal anomaly syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3321533010 | Cardiomyopathy and renal anomaly syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
3321534016 | The association of hypertrophic cardiomyopathy with variable malformations of the urogenital tract. To date, it has been described in two brothers born to nonconsanguineous parents. One of the brothers also had dysgenesis of the corpus callosum. The mode of transmission is unknown but may be X-linked or autosomal recessive. | en | Definition | Inactive | 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