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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

Vertaling van "Hereditary hypogammaglobulinaemia " (Engels → Nederlands) :

Hereditary hypogammaglobulinaemia
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
hereditaire hypogammaglobulinemie
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
hereditary disposition | hereditary predisposition
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
erfelijke aanleg
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Bessel-Hagen disease | hereditary deforming chondrodysplasia | hereditary multiple exostosis | multiple cartilaginous exostoses | multiple exostosis | multiple osteochondromas
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
heriditaire multiple exostose | multiple erfelijk osteochondroom | HME [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
hypogammaglobulinaemia syndrome
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
hypogammaglobulinemie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Nonfamilial hypogammaglobulinaemia
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
niet-familiale hypogammaglobulinemie
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinaemia [CVAgamma] Hypogammaglobulinaemia NOS
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
agammaglobulinemie met immunoglobulinedragende B-lymfocyten | 'common variable'-agammaglobulinemie [CVA-gamma] | hypogammaglobulinemie NNO
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
congenitale chronische diarree met proteïneverliezende enteropathie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
erfelijke plaatsspecifieke eierstokkanker-syndroom
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
diagnosis and management of hereditary disorders | medical genetics
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
medische genetica
https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]
https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndroom van Buschke-Fischer-Brauer
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : bessel-hagen disease     cvagamma     hereditary deforming chondrodysplasia     hereditary disposition     hereditary multiple exostosis     hereditary predisposition     medical genetics     multiple cartilaginous exostoses     multiple exostosis     multiple osteochondromas     Hereditary hypogammaglobulinaemia     


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'Hereditary hypogammaglobulinaemia' ->

Date index: 2023-06-25
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