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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 (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module Reference Sets
53211014 CREST syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
53213012 Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly AND telangiectasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core US English: Acceptable (foundation metadata concept)
485057012 Calcinosis cutis, Raynaud's, oesophageal dysfunction, sclerodactyly AND telangiectasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
1216390014 CREST - Calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
1216391013 CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
1217889016 CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core US English: Acceptable (foundation metadata concept)
1217890013 CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core US English: Acceptable (foundation metadata concept)
2620579016 Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
2620580018 Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core US English: Acceptable (foundation metadata concept)
2837942017 Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core US English: Acceptable (foundation metadata concept)
2913772010 Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Preferred (foundation metadata concept)
2914874013 Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core US English: Acceptable (foundation metadata concept)
3784528011 Calcinosis, Raynaud phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
3784529015 Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core GB English: Acceptable (foundation metadata concept)
1114261000052112 CREST-syndrom sv Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept) Swedish [International Organization for Standardization 639-1 code sv] language reference set (foundation metadata concept): Preferred (foundation metadata concept)

0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
CREST syndrome Is a Secondary Raynaud's phenomenon true Inferred relationship Some
CREST syndrome Is a Acrosclerosis false Inferred relationship Some
CREST syndrome Is a Vascular disease of the skin false Inferred relationship Some
CREST syndrome Is a Calcinosis cutis true Inferred relationship Some
CREST syndrome Associated morphology Sclerosis false Inferred relationship Some 2
CREST syndrome Finding site Structure of fascia (body structure) false Inferred relationship Some 2
CREST syndrome Finding site Connective tissue structure false Inferred relationship Some
CREST syndrome Finding site Structure of artery of extremity false Inferred relationship Some
CREST syndrome Associated morphology Deposition false Inferred relationship Some 2
CREST syndrome Finding site Skin of digit false Inferred relationship Some 1
CREST syndrome Finding site Structure of skin region false Inferred relationship Some 1
CREST syndrome Finding site Skin structure true Inferred relationship Some 2
CREST syndrome Associated morphology Telangiectasis true Inferred relationship Some 5
CREST syndrome Associated morphology Pathologic calcification false Inferred relationship Some 1
CREST syndrome Finding site Connective tissue false Inferred relationship Some
CREST syndrome Is a Sclerosis of the skin false Inferred relationship Some
CREST syndrome Is a Site-specific disorder of skin false Inferred relationship Some
CREST syndrome Is a Disorder of digit true Inferred relationship Some
CREST syndrome Is a Systemic sclerosis with limited cutaneous involvement true Inferred relationship Some
CREST syndrome Is a Disorder of soft tissue of limb false Inferred relationship Some
CREST syndrome Finding site Structure of collagen fibers of skin false Inferred relationship Some
CREST syndrome Is a Disorder of hand (disorder) true Inferred relationship Some
CREST syndrome Finding site Hand structure true Inferred relationship Some 3
CREST syndrome Finding method (attribute) Procedure false Inferred relationship Some
CREST syndrome Interprets Body color false Inferred relationship Some
CREST syndrome Interprets Color of skin false Inferred relationship Some
CREST syndrome Has definitional manifestation Immune system finding false Inferred relationship Some
CREST syndrome Pathological process (attribute) Autoimmune process false Inferred relationship Some
CREST syndrome Finding site Skin of digit true Inferred relationship Some 1
CREST syndrome Associated morphology Pathologic calcification true Inferred relationship Some 1
CREST syndrome Associated morphology Sclerosis false Inferred relationship Some 2
CREST syndrome Finding site Structure of fascia (body structure) false Inferred relationship Some 2
CREST syndrome Is a Autoimmune skin disease false Inferred relationship Some
CREST syndrome Associated morphology Fibrosis false Inferred relationship Some
CREST syndrome Associated morphology Dystrophic calcification true Inferred relationship Some 2
CREST syndrome Is a Systemic disease affecting skin (disorder) true Inferred relationship Some
CREST syndrome Associated morphology Fibrosis true Inferred relationship Some 4
CREST syndrome Finding site Connective tissue structure true Inferred relationship Some 4
CREST syndrome Pathological process (attribute) Autoimmune process true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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