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Atrophie optique autosomique dominante classique
Leucémie mastocytaire classique
Lymphome de Hodgkin classique
Maladie du sirop d'érable classique
Mycosis fongoïde classique
Phénylcétonurie classique
Syndrome d'Ehlers-Danlos classique

Translation of "phénylcétonurie classique " (French → English) :

phénylcétonurie classique
https://browser.ihtsdotools.or (...) (...) [HTML]
PAH deficiency
SNOMEDCT-BE (disorder) / 7573000
SNOMEDCT-BE (disorder) / 7573000
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Phénylcétonurie classique
https://icd.who.int/browse10/2 (...) (...) [HTML]
Classical phenylketonuria
WORLD HEALTH ORGANIZATION ICD-10: E70.0
WORLD HEALTH ORGANIZATION ICD-10: E70.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
atrophie optique autosomique dominante classique
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant optic atrophy Kjer type
SNOMEDCT-BE (disorder) / 717336005
SNOMEDCT-BE (disorder) / 717336005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
mycosis fongoïde classique
https://browser.ihtsdotools.or (...) (...) [HTML]
Classical mycosis fungoides is the most common type of mycosis fungoides, a form of cutaneous T-cell lymphoma, and is characterised by slow progression from patches to more infiltrated plaques and eventually to tumours. The disease first manifests by
SNOMEDCT-BE (disorder) / 765328000
SNOMEDCT-BE (disorder) / 765328000
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
leucémie mastocytaire classique
https://browser.ihtsdotools.or (...) (...) [HTML]
Classic mast cell leukemia
SNOMEDCT-BE (disorder) / 780841002
SNOMEDCT-BE (disorder) / 780841002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
syndrome d'Ehlers-Danlos classique
https://browser.ihtsdotools.or (...) (...) [HTML]
Ehlers-Danlos syndrome classic type
SNOMEDCT-BE (disorder) / 715318006
SNOMEDCT-BE (disorder) / 715318006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie de Pelizaeus-Merzbacher, forme classique
https://browser.ihtsdotools.or (...) (...) [HTML]
Type I classic Pelizaeus-Merzbacher disease
SNOMEDCT-BE (disorder) / 87607002
SNOMEDCT-BE (disorder) / 87607002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
maladie du sirop d'érable classique
https://browser.ihtsdotools.or (...) (...) [HTML]
Severe branched chain ketoacid dehydrogenase deficiency
SNOMEDCT-BE (disorder) / 54064006
SNOMEDCT-BE (disorder) / 54064006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
lymphome de Hodgkin classique
https://browser.ihtsdotools.or (...) (...) [HTML]
Classical Hodgkin lymphoma
SNOMEDCT-BE (disorder) / 762690000
SNOMEDCT-BE (disorder) / 762690000
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
hyperplasie congénitale des surrénales par déficit en 21-hydroxylase classique
https://browser.ihtsdotools.or (...) (...) [HTML]
The most common form of congenital adrenal hyperplasia, divided into 2 clinical groups simple virilising or salt wasting forms. Manifests with genital ambiguity in females and with adrenal insufficiency in both sexes. Girls present with ambiguous gen
SNOMEDCT-BE (disorder) / 717261006
SNOMEDCT-BE (disorder) / 717261006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : phénylcétonurie classique    atrophie optique autosomique dominante classique    leucémie mastocytaire classique    lymphome de hodgkin classique    maladie du sirop d'érable classique    mycosis fongoïde classique    syndrome d'ehlers-danlos classique    


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phénylcétonurie classique

Date index:2023-04-11 -

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