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Encéphalite+
G22
Groupe des 22
Groupe des Vingt-deux
M-22
Monosomie 22
Mouvement du 22 février
Méningite+
Névrite acoustique+
PCC
Parkinsonisme syphilitique+
Parti communiste congolais
Polynévrite+
R48-20-22
R482022
Rétrobulbaire+
Syphilitique tardive
Trisomie 22 en mosaïque
Trisomie partielle du chromosome 22

Translation of "g22 g-22 " (French → English) :

Groupe des Vingt-deux [ G22,G-22 | Groupe des 22 ]

Group of Twenty-Two [ G22,G-22 | Group of 22 ]
Organismes et comités internationaux | Finances
International Bodies and Committees | Finance


Groupe des 22 | G22 [Abbr.]

Group of 22 | G22 [Abbr.]
IATE - FINANCE
IATE - FINANCE


Arthropathie de Charcot+ (M14.6*) Atrophie optique+ (H48.0*) | Encéphalite+ (G05.0*) | Méningite+ (G01*) | Névrite:acoustique+ (H94.0*) | rétrobulbaire+ (H48.1*) | Polynévrite+ (G63.0*) | syphilitique tardive | Parkinsonisme syphilitique+ (G22*) Tabès

Charcot's arthropathy+ (M14.6*) Late syphilitic:acoustic neuritis+ (H94.0*) | encephalitis+ (G05.0*) | meningitis+ (G01*) | optic atrophy+ (H48.0*) | polyneuropathy+ (G63.0*) | retrobulbar neuritis+ (H48.1*) | Syphilitic parkinsonism+ (G22*) Tabes dorsalis
WORLD HEALTH ORGANIZATION ICD-10: A52.1
WORLD HEALTH ORGANIZATION ICD-10: A52.1


Mouvement du 22 février | Parti communiste congolais | M-22 [Abbr.] | PCC [Abbr.]

February 22 Movement | M-22 [Abbr.]
IATE - 04, 0406
IATE - 04, 0406


nocif: risque d'effets graves pour la santé en cas d'exposition prolongée par inhalation et par ingestion | R48/20/22 | R482022 | R48-20-22

harmful:danger of serious damage to health by prolonged exposure through inhalation and if swallowed | R48/20/22
IATE -
IATE -


trisomie 22 en mosaïque

A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are prenatal and postnatal growth delay, mild to severe intellectual disability, hemiatrophy, webbed neck, ocular and cutaneous pigmentary anomalies, cran
SNOMEDCT-BE (disorder) / 764625002
SNOMEDCT-BE (disorder) / 764625002


trisomie partielle du chromosome 22

Duplication of chromosome 22
SNOMEDCT-BE (disorder) / 726362005
SNOMEDCT-BE (disorder) / 726362005


monosomie 22

Deletion 22
SNOMEDCT-BE (disorder) / 787411009
SNOMEDCT-BE (disorder) / 787411009




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g22 g-22

Date index:2023-11-03 -

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