Autosomal recessive agammaglobulinaemia (Swiss type) X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency)

WORLD HEALTH ORGANIZATION ICD-10: D80.0

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agammaglobulinémie

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agammaglobulinaemia [ agammaglobulinemia ]

Maladies des animaux

Animal Diseases

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agammaglobulinémie

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agammaglobulinaemia

médecine

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agammaglobulinémie | absence / insuffisance de gammaglobulines plasmatiques

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agammaglobulinaemia | immune deficiency

UGENT - Medical terms -

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agammaglobulinémie

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agammaglobulinemia

IATE - Health

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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

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agammaglobulinémie liée à l'X

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X-linked agammaglobulinemia

SNOMEDCT-BE (disorder) / 65880007

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Agammaglobulinémie:avec lymphocytes B porteurs d'immunoglobulines | commune variable | Hypogammaglobulinémie SAI

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Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinaemia [CVAgamma] Hypogammaglobulinaemia NOS

WORLD HEALTH ORGANIZATION ICD-10: D80.1

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agammaglobulinémie de bruton

Date index:2021-01-07 -

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Translation of "agammaglobulinémie de bruton " (French → English) :

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