2021000195106: Swiss French language reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Language type reference set (foundation metadata concept)\French [International Organization for Standardization 639-1 code fr] language reference set (foundation metadata concept)\Swiss French language reference set (foundation metadata concept)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 07-Jun 2023. Module: SNOMED CT Switzerland NRC maintained Module

Descriptions:

Id Description Lang Type Status Case? Module

2061000195115 Swiss French language reference set (foundation metadata concept) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2071000195114 Swiss French language reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

237201000195110 ensemble de référence pour la langue française suisse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Swiss French language reference set (foundation metadata concept)	Is a	French [International Organization for Standardization 639-1 code fr] language reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	acceptabilityId
CCR (carcinome à cellules rénales) à cellules claires d'origine métastatique	Acceptable (foundation metadata concept)
CCV - cutaneous collagenous vasculopathy	Acceptable (foundation metadata concept)
CDA - congenital dyserythropoietic anemia	Acceptable (foundation metadata concept)
CDC Corynebacterium group ANF	Acceptable (foundation metadata concept)
CDC Corynebacterium groupe F-1	Preferred (foundation metadata concept)
CDC Corynebacterium groupe I-1	Preferred (foundation metadata concept)
CDG-IIc - leukocyte adhesion deficiency type II	Acceptable (foundation metadata concept)
CDG1A (congenital disorder of glycosylation, type 1a)	Acceptable (foundation metadata concept)
CDG1C (congenital disorder of glycosylation, type 1c)	Acceptable (foundation metadata concept)
CDG1E (congenital disorder of glycosylation, type 1e)	Acceptable (foundation metadata concept)
CDG1F (congenital disorder of glycosylation, type 1f)	Acceptable (foundation metadata concept)
CDG1G (congenital disorder of glycosylation, type 1g)	Acceptable (foundation metadata concept)
CDG1I (congenital disorder of glycosylation, type 1i)	Acceptable (foundation metadata concept)
CDG1J (congenital disorder of glycosylation, type 1j)	Acceptable (foundation metadata concept)
CDG1N (congenital disorder of glycosylation, type 1n)	Acceptable (foundation metadata concept)
CDG1P (congenital disorder of glycosylation, type 1p)	Acceptable (foundation metadata concept)
CDG1Q (congenital disorder of glycosylation, type 1q)	Acceptable (foundation metadata concept)
CDG1R (congenital disorder of glycosylation, type 1r)	Acceptable (foundation metadata concept)
CDG1S (congenital disorder of glycosylation, type 1s)	Acceptable (foundation metadata concept)
CDG1W (congenital disorder of glycosylation, type 1w)	Acceptable (foundation metadata concept)
CDG1X (congenital disorder of glycosylation, type 1x)	Acceptable (foundation metadata concept)
CDG1Y (congenital disorder of glycosylation, type 1y)	Acceptable (foundation metadata concept)
CDG2E (congenital disorder of glycosylation, type 2e)	Acceptable (foundation metadata concept)
CDG2G (congenital disorder of glycosylation, type 2g)	Acceptable (foundation metadata concept)
CDG2H (congenital disorder of glycosylation, type 2h)	Acceptable (foundation metadata concept)
CDG2I (congenital disorder of glycosylation, type 2i)	Acceptable (foundation metadata concept)
CDG2J (congenital disorder of glycosylation, type 2j)	Acceptable (foundation metadata concept)
CDG2O (congenital disorder of glycosylation, type 2o)	Acceptable (foundation metadata concept)
CDH - congenital diaphragmatic hernia	Acceptable (foundation metadata concept)
CDHS - craniofacial deafness hand syndrome	Acceptable (foundation metadata concept)
CE (cholangite à éosinophiles)	Acceptable (foundation metadata concept)
CEC (carcinome épidermoïde cutané) acantholytique	Acceptable (foundation metadata concept)
CEC - celiac disease, epilepsy, cerebral calcification syndrome	Acceptable (foundation metadata concept)
CED - cranioectodermal dysplasia	Acceptable (foundation metadata concept)
CEFS - chirurgie endoscopique fonctionnelle des sinus	Acceptable (foundation metadata concept)
CEP - congenital erythropoietic porphyria	Acceptable (foundation metadata concept)
CFA (conflit fémoroacétabulaire) de l'articulation de la hanche droite	Acceptable (foundation metadata concept)
CFA (conflit fémoroacétabulaire) de l'articulation de la hanche gauche	Acceptable (foundation metadata concept)
CFND - craniofrontonasal dysplasia	Acceptable (foundation metadata concept)
CGD - chronic granulomatous disease	Acceptable (foundation metadata concept)
CGMH (concentration globulaire moyenne en hémoglobine) basse	Acceptable (foundation metadata concept)
CGMH (concentration globulaire moyenne en hémoglobine) normale	Acceptable (foundation metadata concept)
CGMH (concentration globulaire moyenne en hémoglobine) élevée	Acceptable (foundation metadata concept)
CHC (carcinome hépatocellulaire) chez l'adulte	Acceptable (foundation metadata concept)
CHC (carcinome hépatocellulaire) chez l'enfant	Acceptable (foundation metadata concept)
CHC (carcinome hépatocellulaire) fibrolamellaire primitif	Acceptable (foundation metadata concept)
CHC (carcinome hépatocellulaire) primitif	Acceptable (foundation metadata concept)
CHCF - carcinome hépatocellulaire fibrolamellaire	Acceptable (foundation metadata concept)
CHED (congenital hereditary endothelial dystrophy) autosomique dominante	Acceptable (foundation metadata concept)
CHED (congenital hereditary endothelial dystrophy) autosomique récessive	Acceptable (foundation metadata concept)
CHED - congenital hereditary endothelial dystrophy	Acceptable (foundation metadata concept)
CHM - choroïdérémie	Acceptable (foundation metadata concept)
CHP - cytophagic histiocytic panniculitis	Acceptable (foundation metadata concept)
CHSLD - centre d'hébergement et de soins de longue durée	Preferred (foundation metadata concept)
CHU - centre hospitalier universitaire	Preferred (foundation metadata concept)
CIA (communication interauriculaire) par l'orifice du sinus coronaire	Acceptable (foundation metadata concept)
CID par déficit en MAGT1	Acceptable (foundation metadata concept)
CIDP - polyneuropathie démyélinisante inflammatoire chronique	Acceptable (foundation metadata concept)
CIE - congenital non-bullous ichthyosiform erythroderma	Acceptable (foundation metadata concept)
CIPO - chronic intestinal pseudoobstruction	Acceptable (foundation metadata concept)
CIS (carcinome in situ) papillaire du sein	Acceptable (foundation metadata concept)
CISS - cold-induced sweating syndrome	Acceptable (foundation metadata concept)
CIV (communication interventriculaire) acquise	Acceptable (foundation metadata concept)
CIV (communication interventriculaire) périmembraneuse basale centrale	Acceptable (foundation metadata concept)
CIV (communication interventriculaire) récurrente après une procédure	Acceptable (foundation metadata concept)
CIV (communication interventriculaire) récurrente postprocédurale	Acceptable (foundation metadata concept)
CIV (communication interventriculaire) résiduelle après une procédure	Acceptable (foundation metadata concept)
CIV (communication interventriculaire) résiduelle postprocédurale	Acceptable (foundation metadata concept)
CIVD (coagulation intravasculaire disséminée) causée par le venin de serpent	Acceptable (foundation metadata concept)
CIVD (coagulation intravasculaire disséminée) due à un placenta abruptio	Acceptable (foundation metadata concept)
CIVD - coagulation intravasculaire disséminée	Acceptable (foundation metadata concept)
CLIS (carcinome lobulaire in situ) du sein droit	Acceptable (foundation metadata concept)
CLIS (carcinome lobulaire in situ) du sein gauche	Acceptable (foundation metadata concept)
CLL (chaine légère libre) lambda monoclonale présente	Acceptable (foundation metadata concept)
CLL (chaine légère libre) monoclonale présente	Acceptable (foundation metadata concept)
CLN (céroïde-lipofuscinose neuronale) due à un déficit en cathepsine D	Acceptable (foundation metadata concept)
CLN (céroïde-lipofuscinose neuronale) infantile	Acceptable (foundation metadata concept)
CLN (céroïde-lipofuscinose neuronale) juvénile	Acceptable (foundation metadata concept)
CLN infantile tardive	Acceptable (foundation metadata concept)
CLN, variante épilepsie nordique	Acceptable (foundation metadata concept)
CLSC	Acceptable (foundation metadata concept)
CLWM - cystic leukoencephalopathy without megalencephaly	Acceptable (foundation metadata concept)
CM (coma myxœdémateux) dû à une hypothyroïdie subclinique	Acceptable (foundation metadata concept)
CM (coma myxœdémateux) iatrogène	Acceptable (foundation metadata concept)
CMC - carboxyméthylcellulose	Acceptable (foundation metadata concept)
CMC - chronic mucocutaneous candidiasis	Acceptable (foundation metadata concept)
CMD1B - congenital muscular dystrophy type 1B	Acceptable (foundation metadata concept)
CMDH - congenital muscular dystrophy with hyperlaxity	Acceptable (foundation metadata concept)
CME (carcinome mucoépidermoïde) de la glande parotide	Acceptable (foundation metadata concept)
CME (carcinome mucoépidermoïde) de la glande salivaire	Acceptable (foundation metadata concept)
CMF - choroïdite multifocale	Acceptable (foundation metadata concept)
CMH (cardiomyopathie hypertrophique) apicale	Acceptable (foundation metadata concept)
CMP - cardiomyopathie	Acceptable (foundation metadata concept)
CMRD - chylomicron retention disease	Acceptable (foundation metadata concept)
CMT (charge mutationnelle tumorale) faible	Acceptable (foundation metadata concept)
CMT (charge mutationnelle tumorale) élevée	Acceptable (foundation metadata concept)
CMT1A - Charcot-Marie-Tooth disease type 1A	Acceptable (foundation metadata concept)
CMT1B - Charcot-Marie-Tooth disease type 1B	Acceptable (foundation metadata concept)
CMT1C - Charcot-Marie-Tooth disease type 1C	Acceptable (foundation metadata concept)
CMT1D - Charcot-Marie-Tooth disease type 1D	Acceptable (foundation metadata concept)
CMT1F - Charcot-Marie-Tooth disease type 1F	Acceptable (foundation metadata concept)

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
2061000195115	Swiss French language reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
2071000195114	Swiss French language reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
237201000195110	ensemble de référence pour la langue française suisse	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module