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Terminology chevron_right Concepts chevron_right 31848007

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Component

31848007

The component that hold information about this concept.

Fully Specified Name (FSN)

Calcinosis, raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (crest) syndrome (disorder)

Shortest Term

Crest syndrome

Definition Status

900000000000074008 |Necessary but not sufficient concept definition status (core metadata concept)|

Specifies if the concept version is primitive or defined. Set to a descendant of 900000000000444006

Summary

Calcinosis, raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (crest) syndrome (disorder)

SCTID: 31848007, Primitive, Active

31848007|Calcinosis, raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (crest) syndrome (disorder)|

en Calcinosis, raynaud phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (crest) syndrome
en Calcinosis, raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia syndrome
en Calcinosis, raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome
en Calcinosis, raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder)
en Calcinosis, raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (crest) syndrome
en Calcinosis, raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (crest) syndrome
en Calcinosis, raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (crest) syndrome
en Crest - calcinosis, raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia
en Crest - calcinosis, raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia
en Crest - calcinosis, raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndrome
en Crest - calcinosis, raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syndrome
en Calcinosis cutis, raynaud's, esophageal dysfunction, sclerodactyly and telangiectasia
en Calcinosis cutis, raynaud's, oesophageal dysfunction, sclerodactyly and telangiectasia
en Crest syndrome

Expression

31848007 |Calcinosis, raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (crest) syndrome (disorder)|
 <<< 356198000 |Secondary raynaud's phenomenon (disorder)| + 
21323007 |Calcinosis cutis (disorder)| + 
128597007 |Disorder of digit (disorder)| + 
298285004 |Systemic sclerosis with limited cutaneous involvement (disorder)| + 
280134004 |Disorder of soft tissue of limb (disorder)| + 
238980001 |Systemic disease affecting skin (disorder)| + 
363056008 |Degenerative disorder of extremity (disorder)| + 
27550009 |Disorder of blood vessel (disorder)| : 
        { 116676008 |Associated morphology (attribute)| = 18115005 |Pathologic calcification, calcified structure (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 279064005 |Skin of digit (body structure)| }
        { 363698007 |Finding site (attribute)| = 51833009 |Peripheral blood vessel structure (body structure)| }
        { 116676008 |Associated morphology (attribute)| = 112674009 |Fibrosis (morphologic abnormality)|,
363698007 |Finding site (attribute)| = 21793004 |Connective tissue structure (body structure)|,
370135005 |Pathological process (attribute)| = 263680009 |Autoimmune process (qualifier value)| }
        { 116676008 |Associated morphology (attribute)| = 112641009 |Telangiectasis (morphologic abnormality)| }
        

Diagram

Active

Component help	Language Code help	Type	Term help	Case Significance help	Acceptability	Active
3784528011 - Calcinosis, Raynaud phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome (en) View
3784528011	en	Synonym (core metadata concept)	Calcinosis, Raynaud phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
3784529015 - Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia syndrome (en) View
3784529015	en	Synonym (core metadata concept)	Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
2611876012 - Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome (disorder) (en) View
2611876012	en	Fully specified name (core metadata concept)	Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	False
2914874013 - Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (en) View
2914874013	en	Synonym (core metadata concept)	Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
2913772010 - Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder) (en) View
2913772010	en	Fully specified name (core metadata concept)	Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia syndrome (disorder)	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Preferred	True
2837942017 - Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome (en) View
2837942017	en	Synonym (core metadata concept)	Calcinosis, Raynaud phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
2620580018 - Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome (en) View
2620580018	en	Synonym (core metadata concept)	Calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
2620579016 - Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome (en) View
2620579016	en	Synonym (core metadata concept)	Calcinosis, Raynaud's phenomenon, oesophageal dysmotility, sclerodactyly, and telangiectasia (CREST) syndrome	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
763063017 - CREST syndrome (disorder) (en) View
763063017	en	Fully specified name (core metadata concept)	CREST syndrome (disorder)	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	False
1217889016 - CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia (en) View
1217889016	en	Synonym (core metadata concept)	CREST - Calcinosis, Raynaud's phenomenon, esophageal dysfunction, sclerodactyly, telangiectasia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
1216390014 - CREST - Calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia (en) View
1216390014	en	Synonym (core metadata concept)	CREST - Calcinosis, Raynaud's phenomenon, oesophageal dysfunction, sclerodactyly, telangiectasia	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
1217890013 - CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndrome (en) View
1217890013	en	Synonym (core metadata concept)	CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, esophageal involvement, telangiectasia syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
1216391013 - CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syndrome (en) View
1216391013	en	Synonym (core metadata concept)	CREST - Calcinosis, Raynaud's phenomenon, sclerodactyly, oesophageal involvement, telangiectasia syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Acceptable	True
53212019 - Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly and telangiectasia (en) View
53212019	en	Synonym (core metadata concept)	Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly and telangiectasia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	False
53213012 - Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly AND telangiectasia (en) View
53213012	en	Synonym (core metadata concept)	Calcinosis cutis, Raynaud's, esophageal dysfunction, sclerodactyly AND telangiectasia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
485057012 - Calcinosis cutis, Raynaud's, oesophageal dysfunction, sclerodactyly AND telangiectasia (en) View
485057012	en	Synonym (core metadata concept)	Calcinosis cutis, Raynaud's, oesophageal dysfunction, sclerodactyly AND telangiectasia	900000000000020002 \|Only initial character case insensitive (core metadata concept)\|	Acceptable	True
53211014 - CREST syndrome (en) View
53211014	en	Synonym (core metadata concept)	CREST syndrome	900000000000017005 \|Entire term case sensitive (core metadata concept)\|	Preferred	True

Type help	Destination help	Relationship group help	Characteristic type help	Active
Relationship (15143057020) - 31848007 -> 49601007 (116680003) View
116680003 \|Is a (attribute)\|	49601007 \|Disorder of cardiovascular system (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (16405018021) - 31848007 -> 27550009 (116680003) View
116680003 \|Is a (attribute)\|	27550009 \|Disorder of blood vessel (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2545897024) - 31848007 -> 280134004 (116680003) View
116680003 \|Is a (attribute)\|	280134004 \|Disorder of soft tissue of limb (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (16295612020) - 31848007 -> 363056008 (116680003) View
116680003 \|Is a (attribute)\|	363056008 \|Degenerative disorder of extremity (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (751501025) - 31848007 -> 39937001 (363698007) View
363698007 \|Finding site (attribute)\|	39937001 \|Skin structure (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (7078080020) - 31848007 -> 60963005 (116676008) View
116676008 \|Associated morphology (attribute)\|	60963005 \|Dystrophic calcification, calcified structure (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2841687023) - 31848007 -> 118933004 (116680003) View
116680003 \|Is a (attribute)\|	118933004 \|Disorder of hand (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2865225023) - 31848007 -> 85562004 (363698007) View
363698007 \|Finding site (attribute)\|	85562004 \|Hand structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (15143058026) - 31848007 -> 51833009 (363698007) View
363698007 \|Finding site (attribute)\|	51833009 \|Peripheral blood vessel structure (body structure)\|	3	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (751502021) - 31848007 -> 112641009 (116676008) View
116676008 \|Associated morphology (attribute)\|	112641009 \|Telangiectasis (morphologic abnormality)\|	5	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3313015026) - 31848007 -> 263680009 (370135005) View
370135005 \|Pathological process (attribute)\|	263680009 \|Autoimmune process (qualifier value)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3579670029) - 31848007 -> 112674009 (116676008) View
116676008 \|Associated morphology (attribute)\|	112674009 \|Fibrosis (morphologic abnormality)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (11510667029) - 31848007 -> 238980001 (116680003) View
116680003 \|Is a (attribute)\|	238980001 \|Systemic disease affecting skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11574085026) - 31848007 -> 112674009 (116676008) View
116676008 \|Associated morphology (attribute)\|	112674009 \|Fibrosis (morphologic abnormality)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11574086025) - 31848007 -> 21793004 (363698007) View
363698007 \|Finding site (attribute)\|	21793004 \|Connective tissue structure (body structure)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (11574087023) - 31848007 -> 263680009 (370135005) View
370135005 \|Pathological process (attribute)\|	263680009 \|Autoimmune process (qualifier value)\|	4	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3562070028) - 31848007 -> 95329006 (116680003) View
116680003 \|Is a (attribute)\|	95329006 \|Autoimmune skin disease (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3313014027) - 31848007 -> 106182000 (363705008) View
363705008 \|Has definitional manifestation (attribute)\|	106182000 \|Immune system finding (finding)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (751499022) - 31848007 -> 279064005 (363698007) View
363698007 \|Finding site (attribute)\|	279064005 \|Skin of digit (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (751503027) - 31848007 -> 18115005 (116676008) View
116676008 \|Associated morphology (attribute)\|	18115005 \|Pathologic calcification, calcified structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3516540029) - 31848007 -> 279064005 (363698007) View
363698007 \|Finding site (attribute)\|	279064005 \|Skin of digit (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (3516541025) - 31848007 -> 18115005 (116676008) View
116676008 \|Associated morphology (attribute)\|	18115005 \|Pathologic calcification, calcified structure (morphologic abnormality)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2731190027) - 31848007 -> 76455009 (363698007) View
363698007 \|Finding site (attribute)\|	76455009 \|Structure of collagen fibers of skin (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3516542021) - 31848007 -> 43846000 (116676008) View
116676008 \|Associated morphology (attribute)\|	43846000 \|Sclerosis (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (3516543027) - 31848007 -> 84820005 (363698007) View
363698007 \|Finding site (attribute)\|	84820005 \|Structure of fascia (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (504446020) - 31848007 -> 43846000 (116676008) View
116676008 \|Associated morphology (attribute)\|	43846000 \|Sclerosis (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (504447027) - 31848007 -> 84820005 (363698007) View
363698007 \|Finding site (attribute)\|	84820005 \|Structure of fascia (body structure)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2865226024) - 31848007 -> 71388002 (418775008) View
418775008 \|Finding method (attribute)\|	71388002 \|Procedure (procedure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2865227026) - 31848007 -> 248472001 (363714003) View
363714003 \|Interprets (attribute)\|	248472001 \|Body color (observable entity)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2949841027) - 31848007 -> 364533002 (363714003) View
363714003 \|Interprets (attribute)\|	364533002 \|Color of skin (observable entity)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (751497024) - 31848007 -> 4146003 (363698007) View
363698007 \|Finding site (attribute)\|	4146003 \|Structure of artery of extremity (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2226960022) - 31848007 -> 238907001 (116680003) View
116680003 \|Is a (attribute)\|	238907001 \|Site-specific disorder of skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (199813026) - 31848007 -> 50803006 (116680003) View
116680003 \|Is a (attribute)\|	50803006 \|Acrosclerosis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (199814021) - 31848007 -> 11263005 (116680003) View
116680003 \|Is a (attribute)\|	11263005 \|Vascular disease of the skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (751496026) - 31848007 -> 21793004 (363698007) View
363698007 \|Finding site (attribute)\|	21793004 \|Connective tissue structure (body structure)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (1985910021) - 31848007 -> 86352002 (116680003) View
116680003 \|Is a (attribute)\|	86352002 \|Sclerosis of the skin (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (2226961021) - 31848007 -> 128597007 (116680003) View
116680003 \|Is a (attribute)\|	128597007 \|Disorder of digit (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (2226962025) - 31848007 -> 298285004 (116680003) View
116680003 \|Is a (attribute)\|	298285004 \|Systemic sclerosis with limited cutaneous involvement (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (751500029) - 31848007 -> 20795001 (363698007) View
363698007 \|Finding site (attribute)\|	20795001 \|Structure of skin region (body structure)\|	1	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (751498025) - 31848007 -> 46595003 (116676008) View
116676008 \|Associated morphology (attribute)\|	46595003 \|Deposition (morphologic abnormality)\|	2	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (751507026) - 31848007 -> 181769001 (363698007) View
363698007 \|Finding site (attribute)\|	181769001 \|Connective tissue (substance)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	False
Relationship (199812020) - 31848007 -> 356198000 (116680003) View
116680003 \|Is a (attribute)\|	356198000 \|Secondary raynaud's phenomenon (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True
Relationship (199815022) - 31848007 -> 21323007 (116680003) View
116680003 \|Is a (attribute)\|	21323007 \|Calcinosis cutis (disorder)\|	0	900000000000011006 \|Inferred relationship (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active
363056008 View
363056008	Degenerative disorder of extremity (disorder)	Degenerative disorder of extremity	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
238980001 View
238980001	Systemic disease affecting skin (disorder)	Systemic disease affecting skin	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
21323007 View
21323007	Calcinosis cutis (disorder)	Calcinosis cutis	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
280134004 View
280134004	Disorder of soft tissue of limb (disorder)	Disorder of soft tissue of limb	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
27550009 View
27550009	Disorder of blood vessel (disorder)	Angiopathy	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
128597007 View
128597007	Disorder of digit (disorder)	Disorder of digit	900000000000073002 \|Sufficiently defined by necessary conditions definition status (core metadata concept)\|	True
298285004 View
298285004	Systemic sclerosis with limited cutaneous involvement (disorder)	Acrosclerosis	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True
356198000 View
356198000	Secondary raynaud's phenomenon (disorder)	Secondary raynaud phenomenon	900000000000074008 \|Necessary but not sufficient concept definition status (core metadata concept)\|	True

Fully Specified Name (FSN)	Shortest Term	Definition Status help	Active

Reference Set help	Map Target help	Map Rule help	Map Advice help	Correlation help	Map Category help
ExtendedMap object (bc7beebf-c74b-5bc4-98d1-ba24bddec61c) View
447562003 \|Icd-10 complex map reference set (foundation metadata concept)\|	M34.1	TRUE	ALWAYS M34.1	447561005 \|Snomed ct source code to target map code correlation not specified (foundation metadata concept)\|	447637006 \|Map source concept is properly classified (foundation metadata concept)\|

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