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 |
| 53211014 | CREST syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 53213012 | Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly AND telangiectasia | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 485057012 | Calcinosis cutis, Raynaud's, oesophageal dysfunction, sclerodactyly AND telangiectasia | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 1216390014 | CREST - Calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 1216391013 | CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 1217889016 | CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 1217890013 | CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndrome | en | Synonym | Active | Entire term case sensitive | SNOMED CT core module |
| 2620579016 | Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 2620580018 | Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 2837942017 | Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 2913772010 | Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) | en | Fully specified name | Active | Only initial character case insensitive | SNOMED CT core module |
| 2914874013 | Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3784528011 | Calcinosis, Raynaud phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 3784529015 | Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Secondary Raynaud's phenomenon | true | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Acrosclerosis | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Vascular disease of the skin | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Calcinosis cutis | true | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Associated morphology | Sclerosis | false | Inferred relationship | Existential restriction modifier | 2 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Structure of fascia | false | Inferred relationship | Existential restriction modifier | 2 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Connective tissue structure | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Structure of artery of extremity | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Associated morphology | Deposition | false | Inferred relationship | Existential restriction modifier | 2 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Skin structure of digit | false | Inferred relationship | Existential restriction modifier | 1 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Structure of skin region | false | Inferred relationship | Existential restriction modifier | 1 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Skin structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Associated morphology | Telangiectasis | true | Inferred relationship | Existential restriction modifier | 5 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Associated morphology | Pathologic calcification, calcified structure | false | Inferred relationship | Existential restriction modifier | 1 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Connective tissue | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Sclerosis of the skin | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Site-specific disorder of skin | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Disorder of digit | true | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Systemic sclerosis with limited cutaneous involvement | true | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Disorder of soft tissue of limb | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Structure of collagen fibers of skin | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Disorder of hand | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Hand structure | false | Inferred relationship | Existential restriction modifier | 3 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding method | Procedure | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Interprets | Body color | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Interprets | Color of skin | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Has definitional manifestation | Immune system finding | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Pathological process | Autoimmune process | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Skin structure of digit | true | Inferred relationship | Existential restriction modifier | 1 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Associated morphology | Pathologic calcification, calcified structure | true | Inferred relationship | Existential restriction modifier | 1 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Associated morphology | Sclerosis | false | Inferred relationship | Existential restriction modifier | 2 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Structure of fascia | false | Inferred relationship | Existential restriction modifier | 2 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Autoimmune skin disease | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Associated morphology | Fibrosis | false | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Associated morphology | Dystrophic calcification, calcified structure | true | Inferred relationship | Existential restriction modifier | 2 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Systemic disease affecting skin | true | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Associated morphology | Fibrosis | true | Inferred relationship | Existential restriction modifier | 4 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Connective tissue structure | true | Inferred relationship | Existential restriction modifier | 4 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Pathological process | Autoimmune process | true | Inferred relationship | Existential restriction modifier | 4 | |
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Is a | Disorder of cardiovascular system | true | Inferred relationship | Existential restriction modifier | ||
| Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome | Finding site | Peripheral vascular system structure | true | Inferred relationship | Existential restriction modifier | 3 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR