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2021000195106: 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


161454 members. Search Members:

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
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)
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)
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)
CISS - cold-induced sweating syndrome Acceptable (foundation metadata concept)
CIVD - coagulation intravasculaire disséminée 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)
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)
CMP - cardiomyopathie Acceptable (foundation metadata concept)
CMRD - chylomicron retention disease 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)
CMT1X - Charcot-Marie-Tooth disease type 1, X-linked Acceptable (foundation metadata concept)
CMT2A1 - Charcot-Marie-Tooth disease type 2A1 Acceptable (foundation metadata concept)
CMT2A2 - Charcot-Marie-Tooth disease type 2A2 Acceptable (foundation metadata concept)
CMT2B - Charcot-Marie-Tooth disease type 2B Acceptable (foundation metadata concept)
CMT2C - Charcot-Marie-Tooth disease type 2C Acceptable (foundation metadata concept)
CMT2D - Charcot-Marie-Tooth disease type 2D Acceptable (foundation metadata concept)
CMT2E - Charcot-Marie-Tooth disease type 2E Acceptable (foundation metadata concept)
CMT2F - Charcot-Marie-Tooth disease type 2F Acceptable (foundation metadata concept)
CMT2G - Charcot-Marie-Tooth disease type 2G Acceptable (foundation metadata concept)
CMT2I - Charcot-Marie-Tooth disease type 2I Acceptable (foundation metadata concept)
CMT2J - Charcot-Marie-Tooth disease type 2J Acceptable (foundation metadata concept)
CMT2K - Charcot-Marie-Tooth disease type 2K Acceptable (foundation metadata concept)
CMT2L - Charcot-Marie-Tooth disease type 2L Acceptable (foundation metadata concept)
CMT2M - Charcot-Marie-Tooth disease type 2M Acceptable (foundation metadata concept)
CMT2N - Charcot-Marie-Tooth disease type 2N Acceptable (foundation metadata concept)
CMT2Q - Charcot-Marie-Tooth disease type 2Q Acceptable (foundation metadata concept)
CMT2R - Charcot-Marie-Tooth disease type 2R Acceptable (foundation metadata concept)
CMT2U - Charcot-Marie-Tooth disease type 2U Acceptable (foundation metadata concept)
CMT3X - Charcot-Marie-Tooth disease type 3, X-linked Acceptable (foundation metadata concept)
CMT4A - Charcot-Marie-Tooth disease type 4A Acceptable (foundation metadata concept)
CMT4B1 - Charcot-Marie-Tooth disease type 4B1 Acceptable (foundation metadata concept)
CMT4B2 - Charcot-Marie-Tooth disease type 4B2 Acceptable (foundation metadata concept)
CMT4C - Charcot-Marie-Tooth disease type 4C Acceptable (foundation metadata concept)
CMT4D - Charcot-Marie-Tooth disease type 4D Acceptable (foundation metadata concept)
CMT4E - Charcot-Marie-Tooth disease type 4E Acceptable (foundation metadata concept)
CMT4F - Charcot-Marie-Tooth disease type 4F Acceptable (foundation metadata concept)
CMT4G - Charcot-Marie-Tooth disease type 4G Acceptable (foundation metadata concept)
CMT4H - Charcot-Marie-Tooth disease type 4H Acceptable (foundation metadata concept)
CMT4J - Charcot-Marie-Tooth disease type 4J Acceptable (foundation metadata concept)
CMT4X - Charcot-Marie-Tooth disease type 4, X-linked Acceptable (foundation metadata concept)
CMT5X - Charcot-Marie-Tooth disease type 5, X-linked Acceptable (foundation metadata concept)
CMT6X - Charcot-Marie-Tooth disease type 6, X-linked Acceptable (foundation metadata concept)
CMTDIA - Charcot-Marie-Tooth disease, dominant intermediate type A Acceptable (foundation metadata concept)
CMTDIB - Charcot-Marie-Tooth disease type B Acceptable (foundation metadata concept)
CMTDIC - Charcot-Marie-Tooth disease type C Acceptable (foundation metadata concept)
CMTDID - Charcot-Marie-Tooth disease type D Acceptable (foundation metadata concept)
CMTDIE - Charcot-Marie-Tooth disease type E Acceptable (foundation metadata concept)
CMTDIF - Charcot-Marie-Tooth disease type F Acceptable (foundation metadata concept)
CMTX2 - Charcot-Marie-Tooth disease type 2, X-linked Acceptable (foundation metadata concept)
CMUSE - cryptogenic multifocal ulcerous stenosing enteritis Acceptable (foundation metadata concept)
CMVIg immunoglobuline anti-cytomégalovirus non spécifié Preferred (foundation metadata concept)
CNM4 - centronuclear myopathy type 4 Acceptable (foundation metadata concept)
CORS - cerebellooculorenal syndrome Acceptable (foundation metadata concept)
COVID-19 Preferred (foundation metadata concept)
COVID-19 aigüe Preferred (foundation metadata concept)
COVID-19 non spécifié Acceptable (foundation metadata concept)
COVID-19 soupçonnée Preferred (foundation metadata concept)
COVID-19 vaccin codant la protéine de spicule recombinante non spécifié Acceptable (foundation metadata concept)
COVID-19 vaccin à l'acide ribonucléique messager non spécifié Acceptable (foundation metadata concept)
COVID-19 vaccin à particules pseudo-virales non spécifié Preferred (foundation metadata concept)
COVID-19 vaccin à vecteur viral non réplicatif non spécifié Acceptable (foundation metadata concept)
COVID-19 vaccin à virus entier inactivé non spécifié Acceptable (foundation metadata concept)
COXPD12 - combined oxidative phosphorylation defect type 12 Acceptable (foundation metadata concept)
COXPD13 - combined oxidative phosphorylation defect type 13 Acceptable (foundation metadata concept)
COXPD14 - combined oxidative phosphorylation defect type 14 Acceptable (foundation metadata concept)
COXPD15 - combined oxidative phosphorylation defect type 15 Acceptable (foundation metadata concept)
COXPD17 - combined oxidative phosphorylation defect type 17 Acceptable (foundation metadata concept)
COXPD2 - combined oxidative phosphorylation defect type 2 Acceptable (foundation metadata concept)
COXPD21 - combined oxidative phosphorylation defect type 21 Acceptable (foundation metadata concept)
COXPD4 - combined oxidative phosphorylation defect type 4 Acceptable (foundation metadata concept)
COXPD7 - combined oxidative phosphorylation defect type 7 Acceptable (foundation metadata concept)
COXPD8 - combined oxidative phosphorylation defect type 8 Acceptable (foundation metadata concept)
COXPD9 - combined oxidative phosphorylation defect type 9 Acceptable (foundation metadata concept)
CPI - chronic pneumonitis of infancy Acceptable (foundation metadata concept)
CPP - central precocious puberty Acceptable (foundation metadata concept)
CPS1D - carbamoyl-phosphate synthetase 1 deficiency Acceptable (foundation metadata concept)
CPT2 - carnitine palmitoyltransferase II deficiency Acceptable (foundation metadata concept)
CRIE - congenital reticular ichthyosiform erythroderma Acceptable (foundation metadata concept)
CSCD - congenital stromal corneal dystrophy Acceptable (foundation metadata concept)
CSS - Coffin-Siris syndrome Acceptable (foundation metadata concept)
CT scan Acceptable (foundation metadata concept)
CT scan du cerveau Preferred (foundation metadata concept)

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