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31848007: syndroom met calcinose, fenomeen van Raynaud, dysmotiliteit van oesofagus, sclerodactylie en teleangiëctasieën (aandoening)

SNOMED CT Concept\Clinical finding (finding)\...

\Skin AND/OR mucosa finding (finding)\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Calcinosis cutis\CREST syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Degenerative skin disorder (disorder)\Skin deposits\Calcinosis cutis\CREST syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Systemic disease affecting skin (disorder)\CREST syndrome
\Skin AND/OR mucosa finding (finding)\Skin finding\Disorder of skin (disorder)\Skin lesion\Calcinosis cutis\CREST syndrome

\Finding of limb structure\Disorder of limb (disorder)\Disorder of digit\CREST syndrome

\Cardiovascular finding\Raynaud's phenomenon\Secondary Raynaud's phenomenon\CREST syndrome
\Cardiovascular finding\Disorder of cardiovascular system (disorder)\CREST syndrome

\Sign\Raynaud's phenomenon\Secondary Raynaud's phenomenon\CREST syndrome

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

53211014 CREST syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
53212019 Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly and telangiectasia en Synonym (core metadata concept) Inactive Only initial character case insensitive (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
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
763063017 CREST syndrome (disorder) en Fully specified name Inactive Entire term case sensitive (core metadata concept) SNOMED CT core
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
2611876012 Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome (disorder) en Fully specified name Inactive Only initial character case insensitive (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
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
491161000146117 CREST-syndroom nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
491171000146111 syndroom met calcinose, fenomeen van Raynaud, dysmotiliteit van oesofagus, sclerodactylie en teleangiëctasieën (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
491191000146110 gelimiteerde systemische sclerose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
593491000146112 syndroom met calcinose, fenomeen van Raynaud, dysmotiliteit van oesofagus, sclerodactylie en teleangiëctasieën nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
606081000146118 CREST nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
8737631000146119 Combinatie van verschijnselen: calcinose (kalkafzetting), Raynaud-fenomeen (verminderde bloedtoevoer), oesofagusdysmotiliteit (slokdarmklachten), sclerodactylie (verharde vingers), teleangiëctasieën (verwijde huidvaatjes). nl Definition Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)

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 limb (body structure)	false	Inferred relationship	Some
CREST syndrome	Associated morphology	Deposition	false	Inferred relationship	Some	2
CREST syndrome	Finding site	Skin structure of digit (body structure)	false	Inferred relationship	Some	1
CREST syndrome	Finding site	Structure of skin region	false	Inferred relationship	Some	1
CREST syndrome	Finding site	Skin structure	false	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)	false	Inferred relationship	Some
CREST syndrome	Finding site	Hand structure	false	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 structure of digit (body structure)	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	false	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
CREST syndrome	Is a	Disorder of cardiovascular system (disorder)	true	Inferred relationship	Some
CREST syndrome	Finding site	Peripheral vascular system structure	true	Inferred relationship	Some	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
53211014	CREST syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
53212019	Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly and telangiectasia	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (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
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
763063017	CREST syndrome (disorder)	en	Fully specified name	Inactive	Entire term case sensitive (core metadata concept)	SNOMED CT core
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
2611876012	Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome (disorder)	en	Fully specified name	Inactive	Only initial character case insensitive (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
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
491161000146117	CREST-syndroom	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
491171000146111	syndroom met calcinose, fenomeen van Raynaud, dysmotiliteit van oesofagus, sclerodactylie en teleangiëctasieën (aandoening)	nl	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
491191000146110	gelimiteerde systemische sclerose	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
593491000146112	syndroom met calcinose, fenomeen van Raynaud, dysmotiliteit van oesofagus, sclerodactylie en teleangiëctasieën	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
606081000146118	CREST	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
8737631000146119	Combinatie van verschijnselen: calcinose (kalkafzetting), Raynaud-fenomeen (verminderde bloedtoevoer), oesofagusdysmotiliteit (slokdarmklachten), sclerodactylie (verharde vingers), teleangiëctasieën (verwijde huidvaatjes).	nl	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)