21000172104: Belgian 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)\Belgian French language reference set (foundation metadata concept)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 15-Mar 2018. Module: Belgian module (core metadata concept)

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Belgian 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
AF : maladie gastro-intestinale	Acceptable (foundation metadata concept)
AF : ostéoporose	Acceptable (foundation metadata concept)
AF : rein polykystique	Acceptable (foundation metadata concept)
AF : rhume des foins	Acceptable (foundation metadata concept)
AF : trouble de la thyroïde	Acceptable (foundation metadata concept)
AF : trouble endocrinien	Acceptable (foundation metadata concept)
AF : tumeur de l'ovaire	Acceptable (foundation metadata concept)
AF : tumeur maligne	Acceptable (foundation metadata concept)
AF : tumeur maligne de l'ovaire	Acceptable (foundation metadata concept)
AF : tumeur maligne du côlon	Acceptable (foundation metadata concept)
AF : tumeur maligne du sein	Acceptable (foundation metadata concept)
AF : épilepsie	Acceptable (foundation metadata concept)
AFLD - stéatose hépatique alcoolique	Acceptable (foundation metadata concept)
AFLP - acute fatty liver of pregnancy	Acceptable (foundation metadata concept)
AFP (alpha-fœtoprotéine) équivoque	Acceptable (foundation metadata concept)
AG - anesthésie générale	Acceptable (foundation metadata concept)
AGEP - acute generalized exanthematous pustulosis	Acceptable (foundation metadata concept)
AHA (anémie hémolytique auto-immune) néonatale	Acceptable (foundation metadata concept)
AHA associée à PHP IA	Acceptable (foundation metadata concept)
AHC - adénome hépatocellulaire	Acceptable (foundation metadata concept)
AICR - accident ischémique cérébral régressif	Acceptable (foundation metadata concept)
AIED (Åland islands eye disease) et albinisme oculaire	Acceptable (foundation metadata concept)
AIED - Åland Islands eye disease	Acceptable (foundation metadata concept)
AINS - anti-inflammatoire non stéroïdien	Acceptable (foundation metadata concept)
AIP (autoimmune pancreatitis) type 1	Acceptable (foundation metadata concept)
AIT - accident ischémique transitoire	Acceptable (foundation metadata concept)
AIT carotidien	Acceptable (foundation metadata concept)
AIT dans le territoire vertébrobasilaire	Acceptable (foundation metadata concept)
AITL - angioimmunoblastic T-cell lymphoma	Acceptable (foundation metadata concept)
AJI (arthrite juvénile idiopathique) causée par une enthésopathie	Acceptable (foundation metadata concept)
AJI (arthrite juvénile idiopathique) indifférenciée	Acceptable (foundation metadata concept)
AJI (arthrite juvénile idiopathique) polyarticulaire	Acceptable (foundation metadata concept)
AJI - arthrite juvénile idiopathique	Acceptable (foundation metadata concept)
AJI - arthrite juvénile idiopathique de forme systémique	Acceptable (foundation metadata concept)
AKV (acrokératose verruciforme) de Hopf	Acceptable (foundation metadata concept)
AL - amylose à chaines légères	Acceptable (foundation metadata concept)
ALCL - anaplastic large cell lymphoma	Acceptable (foundation metadata concept)
ALD (adrénoleucodystrophie) cérébrale liée à l'X de l'enfant	Acceptable (foundation metadata concept)
ALD (adrénoleucodystrophie) de l'adolescent liée au chromosome X	Acceptable (foundation metadata concept)
ALD (adrénoleucodystrophie) liée à l'X	Acceptable (foundation metadata concept)
ALG1-CDG - asparagine-linked glycosylation 1 congenital disorder of glycosylation	Acceptable (foundation metadata concept)
ALG3-CDG - asparagine-linked glycosylation 3 congenital disorder of glycosylation	Acceptable (foundation metadata concept)
ALG8-CDG - asparagine-linked glycosylation 8 congenital disorder of glycosylation	Acceptable (foundation metadata concept)
ALG9-CDG - asparagine-linked glycosylation 9 congenital disorder of glycosylation	Acceptable (foundation metadata concept)
ALPS - autoimmune lymphoproliferative syndrome	Acceptable (foundation metadata concept)
ALPS avec infections virales récurrentes	Acceptable (foundation metadata concept)
ALV - anastomose lymphoveineuse	Acceptable (foundation metadata concept)
AMAN - acute motor axonal neuropathy	Acceptable (foundation metadata concept)
AMC myogénique autosomique récessive	Acceptable (foundation metadata concept)
AMDH - acromesomelic dysplasia Hunter-Thompson type	Acceptable (foundation metadata concept)
AMG (acidurie 3-méthylglutaconique) type I	Acceptable (foundation metadata concept)
AMG3 - acidurie 3-méthylglutaconique type 3	Acceptable (foundation metadata concept)
AMG4 - acidurie 3-méthylglutaconique type 4	Acceptable (foundation metadata concept)
AMG5 - acidurie 3-méthylglutaconique de type 5	Acceptable (foundation metadata concept)
AMG7 - acidurie 3-méthylglutaconique type 7	Acceptable (foundation metadata concept)
AMKL - acute megakaryoblastic leukemia	Acceptable (foundation metadata concept)
AML (acute myeloid leukemia) familiale	Acceptable (foundation metadata concept)
AMR (acidémie méthylmalonique résistante à la vitamine B12) de type mut0	Acceptable (foundation metadata concept)
AMR (acidémie méthylmalonique résistante à la vitamine B12) partielle	Acceptable (foundation metadata concept)
AMRF - action myoclonus-renal failure	Acceptable (foundation metadata concept)
AMTD - anémie mégaloblastique thiamine dépendante	Acceptable (foundation metadata concept)
ANCA (anti neutrophil cytoplasmic antibodies) négatifs	Acceptable (foundation metadata concept)
ANCA (anti neutrophil cytoplasmic antibodies) positifs	Acceptable (foundation metadata concept)
ANCL - adult neuronal ceroid lipofuscinosis	Acceptable (foundation metadata concept)
ANE (acute necrotizing encephalopathy) isolée	Acceptable (foundation metadata concept)
AO1 - atélostéogenèse type I	Acceptable (foundation metadata concept)
AO2 - atélostéogénèse de type 2	Acceptable (foundation metadata concept)
AO3 - atélostéogénèse de type 3	Acceptable (foundation metadata concept)
AOC - albinisme oculo-cutané	Acceptable (foundation metadata concept)
AOC1 - albinisme oculo-cutané type 1	Acceptable (foundation metadata concept)
AOC2	Acceptable (foundation metadata concept)
AOC4 - albinisme oculo-cutané type 4	Acceptable (foundation metadata concept)
AOC5 - albinisme oculo-cutané type 5	Acceptable (foundation metadata concept)
AOC6 - albinisme oculo-cutané type 6	Acceptable (foundation metadata concept)
AOC7 - albinisme oculo-cutané type 7	Acceptable (foundation metadata concept)
AOD+ - atrophie optique dominante plus	Acceptable (foundation metadata concept)
APAC - acute primary angle closure	Acceptable (foundation metadata concept)
APBD - adult polyglucosan body disease	Acceptable (foundation metadata concept)
APDS - activated PI3K-delta syndrome	Acceptable (foundation metadata concept)
APLAID - autoinflammation and PLCG 2-associated antibody deficiency and immune dysregulation	Acceptable (foundation metadata concept)
APP (aphasie primaire progressive) logopénique	Acceptable (foundation metadata concept)
APP (aphasie primaire progressive) non fluente	Acceptable (foundation metadata concept)
APP (aphasie primaire progressive) sémantique	Acceptable (foundation metadata concept)
APS (amblyopie par privation de stimulus) bilatérale	Acceptable (foundation metadata concept)
APS (amblyopie par privation de stimulus) de l'œil droit	Acceptable (foundation metadata concept)
APS (amblyopie par privation de stimulus) de l'œil gauche	Acceptable (foundation metadata concept)
APS (antiphospholipides) néonatal	Acceptable (foundation metadata concept)
AR-CMT1 - autosomal recessive Charcot-Marie-Tooth disease type 4	Acceptable (foundation metadata concept)
AR-CMT2 avec acrodystrophie	Acceptable (foundation metadata concept)
AR-CMT2 type Ouvrier	Acceptable (foundation metadata concept)
AR-CMT2B1 - autosomal recessive Charcot-Marie-Tooth disease type 2B1	Acceptable (foundation metadata concept)
AR-CMT2B2 - autosomal recessive Charcot-Marie-Tooth disease type 2B2	Acceptable (foundation metadata concept)
AR-CMT2B5 - autosomal recessive Charcot-Marie-Tooth disease type 2B5	Acceptable (foundation metadata concept)
AR-CMT2C - autosomal recessive Charcot-Marie-Tooth disease type 2C	Acceptable (foundation metadata concept)
AR-CNM - autosomal recessive centronuclear myopathy	Acceptable (foundation metadata concept)
ARAN-NM - autosomal recessive axonal neuropathy with neuromyotonia	Acceptable (foundation metadata concept)
ARCA2 - autosomal recessive cerebellar ataxia type 2	Acceptable (foundation metadata concept)
ARCL2 type progéroïde	Acceptable (foundation metadata concept)
ARCL2A - autosomal recessive cutis laxa type 2A	Acceptable (foundation metadata concept)
ARCMT2K - autosomal recessive Charcot-Marie-Tooth disease type 2K	Acceptable (foundation metadata concept)
AREB-1 - anémie réfractaire avec excès de blastes type 1	Acceptable (foundation metadata concept)

Start Previous Page 9 of 2522 Next End

Reference Sets

Reference set descriptor

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
31000172117	Belgian French language reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
41000172112	Belgian French language reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)
80741000172111	fichier de référence français belge	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
80721000172119	Belgisch-Frans referentiebestand	nl	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	Belgian module (core metadata concept)