Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3756077015 | Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3756078013 | Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome | Associated morphology | Telangiectasis | true | Inferred relationship | Existential restriction modifier | 1 | |
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome | Finding site | Microscopic skin vascular structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome | Is a | Hereditary disorder of the integument | true | Inferred relationship | Existential restriction modifier | ||
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome | Is a | Telangiectasia disorder | false | Inferred relationship | Existential restriction modifier | ||
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome | Is a | Familial disease | true | Inferred relationship | Existential restriction modifier | ||
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome | Is a | Hereditary cancer-predisposing syndrome | true | Inferred relationship | Existential restriction modifier | ||
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome | Is a | Cardiovascular system hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome | Is a | Telangiectasia of skin | true | Inferred relationship | Existential restriction modifier |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets