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31848007: Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder)

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
53212019 Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly and telangiectasia en Synonym Inactive Only initial character case insensitive 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
763063017 CREST syndrome (disorder) en Fully specified name Inactive Entire term case sensitive 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
2611876012 Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome (disorder) en Fully specified name Inactive Only initial character case insensitive 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

0 descendants.

Expanded Value Set

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

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