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Translation of "VII " (French → Dutch) :
TERMINOLOGY
see also In-Context Translations below Afibrinogénémie congénitale Carence en:AC-globuline | proaccélérine | Carence en facteur:I [fibrinogène] | II [prothrombine] | V [labile] | VII [stable] | X [Stuart-Prower] | XII [Hageman] | XIII [stabilisant de la fibrine] | Disfibrinogénémie (congénitale) Hypoproconvertinémie Maladie de Owren
congenitale afibrinogenemie | deficiëntie van | AC globuline | deficiëntie van | proaccelerine | deficiëntie van factor | I [fibrinogeen] | deficiëntie van factor | II [protrombine] | deficiëntie van factor | V [labiel] | deficiëntie van factor | VII [stabiel] | deficiëntie van factor | X [Stuart-Prower] | deficiëntie van factor | XII [Hageman] | deficiëntie van factor | XIII [fibrinestabiliserend] | dysfibrinogenemie (congenitaal) | hypoproconvertinemie | ziekte van Owren
WORLD HEALTH ORGANIZATION ICD-10: D68.2
WORLD HEALTH ORGANIZATION ICD-10: D68.2
Nerf crânien VII
zevende hersenzenuw [n. VII]
WORLD HEALTH ORGANIZATION ICD-10: S04.5
WORLD HEALTH ORGANIZATION ICD-10: S04.5
affections du nerf crânien VII
aandoeningen van zevende hersenzenuw [n. VII]
WORLD HEALTH ORGANIZATION ICD-10: G51
WORLD HEALTH ORGANIZATION ICD-10: G51
Carence en bêta-glucoronidase Mucopolysaccharidoses, type III, IV, VI, VII Syndrome de:Maroteaux-Lamy (léger) (sévère) | Morquio (-semblable à) (classique) | Sanfilippo (type B) (type C) (type D)
bèta-glucuronidasedeficiëntie | mucopolysaccharidose, type III, IV, VI, VII | syndroom (van) | Maroteaux-Lamy (licht)(ernstig) | syndroom (van) | Morquio(-achtig)(klassiek) | syndroom (van) | Sanfilippo (type B)(type C)(type D)
WORLD HEALTH ORGANIZATION ICD-10: E76.2
WORLD HEALTH ORGANIZATION ICD-10: E76.2
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VII
Date index:2024-03-21 -
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