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31848007: syndrome de CREST (trouble)


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
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
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
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
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
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
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
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
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
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
3393430013 sclérodermie de type Crest fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3393432017 phénomène de Raynaud fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3393501015 syndrome CREST fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core 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
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
400691000172118 syndrome de CREST fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
416911000241112 syndrome de CREST (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core 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
53211014 CREST syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) pathologies systémiques avec manifestations cutanées true Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) morphologie associée (attribut) Fibrosis true Inferred relationship Some 4
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) Connective tissue structure true Inferred relationship Some 4
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) Pathological process (attribute) Autoimmune process true Inferred relationship Some 4
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Disorder of cardiovascular system (disorder) true Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) structure du système vasculaire périphérique true Inferred relationship Some 3
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Sclerosis of the skin false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Secondary Raynaud's phenomenon (finding) true Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Acrosclerosis (disorder) false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Vascular disease of the skin false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Calcinosis cutis true Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Site-specific disorder of skin false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Disorder of digit true Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) sclérose systémique avec atteinte cutanée limitée true Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Disorder of soft tissue of limb false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) Structure of collagen fibers of skin false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Disorder of hand (disorder) false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) main false Inferred relationship Some 3
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) méthode de constatation (attribut) Procedure false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) interprète (attribut) Body color false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) interprète (attribut) Color of skin false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est défini par la manifestation de (attribut) Immune system finding false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) Pathological process (attribute) Autoimmune process false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) Skin of digit true Inferred relationship Some 1
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) morphologie associée (attribut) Pathologic calcification, calcified structure (morphologic abnormality) true Inferred relationship Some 1
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) morphologie associée (attribut) sclérose (anomalie morphologique) false Inferred relationship Some 2
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) Structure of fascia (body structure) false Inferred relationship Some 2
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) est un(e) (attribut) Autoimmune skin disease false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) morphologie associée (attribut) Fibrosis false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) morphologie associée (attribut) sclérose (anomalie morphologique) false Inferred relationship Some 2
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) Structure of fascia (body structure) false Inferred relationship Some 2
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) morphologie associée (attribut) Dystrophic calcification true Inferred relationship Some 2
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) Connective tissue structure false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) Structure of artery of extremity false Inferred relationship Some
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) morphologie associée (attribut) Deposition false Inferred relationship Some 2
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) Skin of digit false Inferred relationship Some 1
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) Structure of skin region false Inferred relationship Some 1
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 2
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) morphologie associée (attribut) Telangiectasis true Inferred relationship Some 5
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) morphologie associée (attribut) Pathologic calcification, calcified structure (morphologic abnormality) false Inferred relationship Some 1
Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) localisation d'une constatation (attribut) Connective tissue false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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