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Birth defect
Bruton's X-linked agammaglobulinemia
Bruton's disease
Bruton's hypogammaglobulinemia
Congenital
Congenital anomaly
Congenital defect
Congenital deformity
Congenital disease
Congenital disorder
Congenital hypogammaglobulinaemia
Congenital hypogammaglobulinemia
Congenital malformation
Early congenital syphilis cutaneous
Early congenital syphilitic laryngitis
From birth
Hypogammaglobulinemia
Mucocutaneous
Oculopathy
Osteochondropathy
Pharyngitis
Pneumonia
Rhinitis
Visceral
X-linked agammaglobulinaemia
XLA

Vertaling van "Congenital hypogammaglobulinemia " (Engels → Nederlands) :

congenital hypogammaglobulinaemia | congenital hypogammaglobulinemia

congenitale hypogammaglobulinemie


birth defect | congenital anomaly | congenital defect | congenital disease | congenital disorder | congenital malformation

aangeboren aandoening


congenital disease [ congenital deformity | congenital malformation ]

aangeboren ziekte [ aangeboren afwijking ]


Bruton's disease | Bruton's hypogammaglobulinemia | Bruton's X-linked agammaglobulinemia | X-linked agammaglobulinaemia | XLA [Abbr.]

Bruton hypogamma globulinemie | ziekte van Bruton


Syndrome that is characterized by the association of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease. Mutations in the gene coding

hepatische veno-occlusieve ziekte, immuundeficiëntie


A rare genetic endocrine disease characterized by the association of common variable immunodeficiency manifesting with hypogammaglobulinemia and recurrent or severe childhood-onset sinopulmonary infections, followed, possibly many years later, by sym

deficiëntie in anterieure hypofysefunctie, variabele immuundeficiëntiesyndroom






Early congenital syphilis:cutaneous | mucocutaneous | visceral | Early congenital syphilitic:laryngitis | oculopathy | osteochondropathy | pharyngitis | pneumonia | rhinitis

Elke congenitale syfilitische aandoening gespecificeerd als vroeg of zich manifesterend binnen twee jaar na geboorte. | vroege congenitalesyfilis | cutaan | vroege congenitalesyfilis | mucocutaan | vroege congenitalesyfilis | visceraal | vroege congenitale syfilitische- | faryngitis | vroege congenitale syfilitische- | oculopathie | - | vroege congenitale syfilitische- | osteochondropathie | vroege congenitale syfilitische- | pneumonie | vroege congenitale syfilitische- | rinitis | vroege congenitale syfilitische- | laryngitis


Late congenital syphilitic interstitial keratitis+ (H19.2*) Late congenital syphilitic oculopathy NEC+ (H58.8*)

late congenitale syfilitische- | interstitiële-keratitis (H19.2) | late congenitale syfilitische- | oculopathie NEC (H58.8)




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'Congenital hypogammaglobulinemia' ->

Date index: 2021-12-04
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