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Aarskog
Acute familiaire haemolyse
Acute familiale hemolyse
Cockayne
De Lange
Dubowitz
Giant platelet syndrome
Grey platelet syndrome
Manisch depressief syndroom
Noonan
Prader-Willi
Robinow-Silverman-Smith
Russell-Silver
Seckel
Smith-Lemli-Opitz
Syndroom
Syndroom van
Syndroom van Bernard
Syndroom van Bernard-Soulier
Syndroom van Horner
Syndroom van Horner-Bernard
Trombasthenie
Trombocytopathie
Ziekte van Glanzmann
Ziektebeeld

Translation of "syndroom van bernard " (Dutch → French) :

syndroom van Bernard | syndroom van Horner | syndroom van Horner-Bernard

syndrome de Bernard | syndrome oculo-sympathique
IATE - Health
IATE - Health


syndroom van Bernard(-Horner)

Pupille de Horner
WORLD HEALTH ORGANIZATION ICD-10: G90.2
WORLD HEALTH ORGANIZATION ICD-10: G90.2


acute familiaire haemolyse | acute familiale hemolyse | syndroom van Bernard

hémolyse de Bernard
IATE - Health
IATE - Health


grey platelet syndrome | syndroom van Bernard-Soulier [giant platelet syndrome] | trombasthenie (hemorragisch)(hereditair) | trombocytopathie | ziekte van Glanzmann

Maladie de Glanzmann Syndrome de(s):Bernard-Soulier [plaquettes géantes] | plaquettes grises | Thrombasthénie (hémorragique) (héréditaire) Thrombopathie
WORLD HEALTH ORGANIZATION ICD-10: D69.1
WORLD HEALTH ORGANIZATION ICD-10: D69.1


syndroom van Horner | syndroom van Horner-Bernard

syndrome de Claude-Bernard-Horner | syndrome oculaire sympathique
IATE - Health
IATE - Health


syndroom | ziektebeeld

syndrome | syndrome
UGENT - Medical terms -
UGENT - Medical terms -


manisch depressief syndroom

maniaco-dépressivité
sciences/technique médecine annexe 2
sciences/technique médecine annexe 2


syndroom van | Aarskog | syndroom van | Cockayne | syndroom van | de Lange | syndroom van | Dubowitz | syndroom van | Noonan | syndroom van | Prader-Willi | syndroom van | Robinow-Silverman-Smith | syndroom van | Russell-Silver | syndroom van | Seckel | syndroom van | Smith-Lemli-Opitz

Syndrome de:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz
WORLD HEALTH ORGANIZATION ICD-10: Q87.1
WORLD HEALTH ORGANIZATION ICD-10: Q87.1


SOLAMEN (segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus)-syndroom

syndrome d'hypertrophie segmentaire-lipomatose-malformation artérioveineuse-naevus épidermique
SNOMEDCT-BE (segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus)-syndroom / 763867001
SNOMEDCT-BE (disorder) / 763867001


AHO-PHP (Albright hereditary osteodystrophy, pseudohypoparathyroidism)-syndroom Ia

pseudohypoparathyroïdie type 1A
SNOMEDCT-BE (Albright hereditary osteodystrophy, pseudohypoparathyroidism)-syndroom Ia / 58833000
SNOMEDCT-BE (disorder) / 58833000




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'syndroom van bernard'

Date index:2022-06-17 -

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