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Aarskog
Cockayne
Congenitaal syndroom van Horner
De Lange
Dubowitz
Manisch depressief syndroom
Noonan
Prader-Willi
Robinow-Silverman-Smith
Russell-Silver
Seckel
Smith-Lemli-Opitz
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Bernard
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Horner
Syndroom van Horner-Bernard

Translation of "Syndroom van Horner " (Dutch → French) :

syndroom van Horner | syndroom van Horner-Bernard

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


syndroom van Horner

Syndrome de Claude Bernard-Horner
WORLD HEALTH ORGANIZATION ICD-10: G90.2
WORLD HEALTH ORGANIZATION ICD-10: G90.2


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

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


congenitaal syndroom van Horner

syndrome de Horner congénital
SNOMEDCT-BE (disorder) / 770626007
SNOMEDCT-BE (disorder) / 770626007


syndroom van Bernard(-Horner)

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


manisch depressief syndroom

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


syndroom van Abderhalden-Fanconi | syndroom van Debré-de Toni-Fanconi | syndroom van Debré-Fanconi

diabète rénal gluco-phosphoaminé | syndrome de De Toni-Debré-Fanconi
IATE - Health
IATE - Health


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


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

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


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




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'Syndroom van Horner'

Date index:2022-11-26 -

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