Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
36695013 | Osler hemorrhagic telangiectasia syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
36696014 | Osler-Weber-Rendu disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
36697017 | Hereditary hemorrhagic telangiectasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
481146013 | Osler-Rendu-Weber syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
481147016 | Osler-Rendu-Weber disease | en | Synonym | Active | Case sensitive | SNOMED CT core |
481148014 | Osler haemorrhagic telangiectasia syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
481149018 | Hereditary haemorrhagic telangiectasia | en | Synonym | Active | Case insensitive | SNOMED CT core |
481150018 | HHT - Hereditary haemorrhagic telangiectasia | en | Synonym | Active | Case sensitive | SNOMED CT core |
481151019 | HHT - Hereditary hemorrhagic telangiectasia | en | Synonym | Active | Case sensitive | SNOMED CT core |
751221018 | Osler hemorrhagic telangiectasia syndrome (disorder) | en | Fully specified name | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Juvenile polyposis syndrome with hereditary haemorrhagic telangiectasia | Is a | True | Osler haemorrhagic telangiectasia syndrome | Inferred relationship | Some | |
Hereditary haemorrhagic telangiectasia of gingiva | Is a | True | Osler haemorrhagic telangiectasia syndrome | Inferred relationship | Some |
Reference Sets
Emergency department reference set
Australian emergency department reference set
NSW Emergency Department reference set
Clinical finding foundation reference set
Cardiovascular finding reference set
Emergency department diagnosis reference set
Problem/Diagnosis reference set