Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
36695013 | Osler hemorrhagic telangiectasia syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
36696014 | Osler-Weber-Rendu disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
36697017 | Hereditary hemorrhagic telangiectasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
481146013 | Osler-Rendu-Weber syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
481147016 | Osler-Rendu-Weber disease | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
481148014 | Osler haemorrhagic telangiectasia syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
481149018 | Hereditary haemorrhagic telangiectasia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
481150018 | HHT - Hereditary haemorrhagic telangiectasia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
481151019 | HHT - Hereditary hemorrhagic telangiectasia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
751221018 | Osler hemorrhagic telangiectasia syndrome (disorder) | en | Fully specified name | Active | Entire term case sensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Juvenile polyposis syndrome with hereditary hemorrhagic telangiectasia | Is a | True | Osler hemorrhagic telangiectasia syndrome | Inferred relationship | Existential restriction modifier | |
Hereditary hemorrhagic telangiectasia of gingiva | Is a | True | Osler hemorrhagic telangiectasia syndrome | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets