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Bessel-Hagen disease
CVAgamma
Diagnosis and management of hereditary disorders
Hereditary deforming chondrodysplasia
Hereditary disposition
Hereditary hypogammaglobulinaemia
Hereditary multiple exostosis
Hereditary predisposition
Hypogammaglobulinaemia NOS
Hypogammaglobulinaemia syndrome
Medical genetics
Multiple cartilaginous exostoses
Multiple exostosis
Multiple osteochondromas
Nonfamilial hypogammaglobulinaemia

Traduction de «hereditary hypogammaglobulinaemia » (Anglais → Néerlandais) :

Hereditary hypogammaglobulinaemia

hereditaire hypogammaglobulinemie


hereditary disposition | hereditary predisposition

erfelijke aanleg


Bessel-Hagen disease | hereditary deforming chondrodysplasia | hereditary multiple exostosis | multiple cartilaginous exostoses | multiple exostosis | multiple osteochondromas

heriditaire multiple exostose | multiple erfelijk osteochondroom | HME [Abbr.]




Nonfamilial hypogammaglobulinaemia

niet-familiale hypogammaglobulinemie


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

agammaglobulinemie met immunoglobulinedragende B-lymfocyten | 'common variable'-agammaglobulinemie [CVA-gamma] | hypogammaglobulinemie NNO


A rare genetic intestinal disease characterised by early-onset chronic non-infectious, non-bloody, watery diarrhoea associated with protein-losing enteropathy, which results in hypoalbuminaemia, hypogammaglobulinaemia and elevated stool alpha-1-antit

congenitale chronische diarree met proteïneverliezende enteropathie


Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec

erfelijke plaatsspecifieke eierstokkanker-syndroom


diagnosis and management of hereditary disorders | medical genetics

medische genetica


A very rare hereditary skin disease with manifestation of irregularly distributed epidermal hyperkeratosis of the palms and soles. Reported in 35 families worldwide to date. The lesions usually start to develop in early adolescence but can also prese

syndroom van Buschke-Fischer-Brauer




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Date index: 2023-05-22
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