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Agammaglobulinémie
Agammaglobulinémie autosomique récessive
Agammaglobulinémie isolée
Agammaglobulinémie liée à l'X
Agammaglobulinémie type Bruton
Bruton
Commune variable
Dysplasie corticale focale isolée
Hypogammaglobulinémie SAI
Liée au chromosome X
Paralysie faciale congénitale héréditaire isolée
Polykystose hépatique isolée

Translation of "Agammaglobulinémie isolée " (French → English) :

agammaglobulinémie isolée
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The non-syndromic form of a primary immunodeficiency disease characterized by deficient gamma globulins and associated predisposition to frequent and recurrent infections from infancy. Two forms have been described: X-linked represents approximately
SNOMEDCT-BE (disorder) / 764858009
SNOMEDCT-BE (disorder) / 764858009
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https://browser.ihtsdotools.or (...) [HTML]
agammaglobulinémie | absence / insuffisance de gammaglobulines plasmatiques
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agammaglobulinaemia | immune deficiency
UGENT - Medical terms -
UGENT - Medical terms -
http://users.ugent.be/~rvdstic (...) (...) [HTML]
http://users.ugent.be/~rvdstic (...) [HTML]
agammaglobulinémie type Bruton
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Bruton's type agammaglobulinemia
SNOMEDCT-BE (disorder) / 65880007
SNOMEDCT-BE (disorder) / 65880007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
agammaglobulinémie liée à l'X
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X-linked agammaglobulinemia
SNOMEDCT-BE (disorder) / 65880007
SNOMEDCT-BE (disorder) / 65880007
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https://browser.ihtsdotools.or (...) [HTML]
Agammaglobulinémie:autosomique récessive (type suisse) | liée au chromosome X [Bruton] (avec déficit de l'hormone de croissance)
https://icd.who.int/browse10/2 (...) (...) [HTML]
Autosomal recessive agammaglobulinaemia (Swiss type) X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency)
WORLD HEALTH ORGANIZATION ICD-10: D80.0
WORLD HEALTH ORGANIZATION ICD-10: D80.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Agammaglobulinémie:avec lymphocytes B porteurs d'immunoglobulines | commune variable | Hypogammaglobulinémie SAI
https://icd.who.int/browse10/2 (...) (...) [HTML]
Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinaemia [CVAgamma] Hypogammaglobulinaemia NOS
WORLD HEALTH ORGANIZATION ICD-10: D80.1
WORLD HEALTH ORGANIZATION ICD-10: D80.1
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
dysplasie corticale focale isolée
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Isolated focal cortical dysplasia
SNOMEDCT-BE (disorder) / 766710005
SNOMEDCT-BE (disorder) / 766710005
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https://browser.ihtsdotools.or (...) [HTML]
hypomagnésémie isolée autosomique dominante type Glaudemans
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Isolated autosomal dominant hypomagnesemia Glaudemans type
SNOMEDCT-BE (disorder) / 722008003
SNOMEDCT-BE (disorder) / 722008003
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https://browser.ihtsdotools.or (...) [HTML]
polykystose hépatique isolée
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A genetic disorder with characteristics of the appearance of numerous cysts spread throughout the liver. Women are predominantly affected and have a larger number of cysts than affected males. Cysts are undetectable early in life and usually appear a
SNOMEDCT-BE (disorder) / 716196007
SNOMEDCT-BE (disorder) / 716196007
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https://browser.ihtsdotools.or (...) [HTML]
paralysie faciale congénitale héréditaire isolée
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An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or a
SNOMEDCT-BE (disorder) / 733091002
SNOMEDCT-BE (disorder) / 733091002
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https://browser.ihtsdotools.or (...) [HTML]


Others have searched : bruton    agammaglobulinémie    agammaglobulinémie isolée    agammaglobulinémie liée à l'x    agammaglobulinémie type bruton    commune variable    dysplasie corticale focale isolée    liée au chromosome    paralysie faciale congénitale héréditaire isolée    polykystose hépatique isolée    Agammaglobulinémie isolée    


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Agammaglobulinémie isolée

Date index:2021-12-03 -

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