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CFNR
CVAgamma
Call forward-no answer
Call forwarding no reply
Congenital hypogammaglobulinaemia
Congenital hypogammaglobulinemia
Hereditary hypogammaglobulinaemia
Hypogammaglobulinaemia NOS
Hypogammaglobulinaemia syndrome
No fault
Nonfamilial hypogammaglobulinaemia

Vertaling van "Hypogammaglobulinaemia NOS " (Engels → Nederlands) :

TERMINOLOGIE
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]
congenital hypogammaglobulinaemia | congenital hypogammaglobulinemia
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
congenitale hypogammaglobulinemie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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]
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]
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]
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]
Call forwarding no reply | Call forward-no answer (États-Unis) | CFNR
http://www.franca.cfwb.be/t000 (...) (...) [HTML] [2018-01-01]
Call forwarding no reply | CFNR | Oproepdoorschakeling
http://www.franca.cfwb.be/t000 (...) (...) [HTML] [2018-01-01]
http://www.franca.cfwb.be/t000 (...) [HTML] [2018-01-01]
A rare and isolated orofacial defect with manifestation of incomplete median clefts of both the lower lip (limited to the vermilion, with no muscle involvement) and upper lip (with muscle involvement), double labial frenulum and fusion of the upper g
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
familiale mediane splijting van boven- en onderlip
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
No fault
http://www.franca.cfwb.be/e000 (...) (...) [HTML] [2018-01-01]
No fault
http://www.franca.cfwb.be/e000 (...) (...) [HTML] [2018-01-01]
http://www.franca.cfwb.be/e000 (...) [HTML] [2018-01-01]
An X-linked disorder of purine metabolism comprised of two forms: an early-onset severe form with characteristics of gout, urolithiasis, and neurodevelopmental anomalies (severe PRPP synthetase superactivity) and a mild late-onset form with no neurol
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
fosforibosylpyrofosfaatsynthetase-superactiviteit
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
IN-CONTEXT TRANSLATIONS
Human normal immunoglobulin (ivig) || Kiovig || 2011 || Extension of indication to include treatment of multifocal motor neuropathy and hypogammaglobulinaemia in patients after allogeneic haematopoietic stem cell transplantation in adults and children
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2002-01-31]
Humaan normaal immunoglobuline (ivig) || Kiovig || 2011 || Uitbreiding van indicatie met opname van behandeling van multifocale motorische neuropathie en hypogammaglobulinemie bij patiënten na allogene hematopoïetische-stamceltransplantatie bij volwassenen en kinderen
https://eur-lex.europa.eu/lega (...) (...) [HTML] [2002-01-31]
https://eur-lex.europa.eu/lega (...) [HTML] [2002-01-31]


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