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Becker
Bessel-Hagen disease
Congenital myotonia
Diagnosis and management of hereditary disorders
Dominant
Drug-induced
Dystrophia myotonica
Hereditary deforming chondrodysplasia
Hereditary disposition
Hereditary multiple exostosis
Hereditary myotonia
Hereditary predisposition
Isaacs
Medical genetics
Multiple cartilaginous exostoses
Multiple exostosis
Multiple osteochondromas
Myotonia chondrodystrophic
Myotonia congenita - autosomal dominant form
Myotonia congenita NOS
Myotonia permanens
Neuromyotonia
Paramyotonia congenita Pseudomyotonia
Recessive
Steinert
Symptomatic
Thomsen
Thomsen disease

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

congenital myotonia | hereditary myotonia | Thomsen disease
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
myotonia congenita | myotonia hereditaria | paramyotonia congenita | ziekte van Thomsen
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Dystrophia myotonica [Steinert] Myotonia:chondrodystrophic | drug-induced | symptomatic | Myotonia congenita:NOS | dominant [Thomsen] | recessive [Becker] | Neuromyotonia [Isaacs] Paramyotonia congenita Pseudomyotonia
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
dystrophia myotonica [Steinert] | myotonia congenita | NNO | myotonia congenita | dominant [Thomsen] | myotonia congenita | recessief [Becker] | myotonie | chondrodystrofisch | myotonie | door geneesmiddelen | myotonie | symptomatisch | neuromyotonie [Isaacs] | pramyotonia congenita | pseudomyotonie
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
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]
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]
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]
Myotonia permanens
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
myotonia permanens
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Myotonia congenita - autosomal dominant form
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
congenitale myotonie, autosomale dominante vorm
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]
Adenomatosis of colon Large intestine NOS Polyposis (hereditary) of colon
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
adenomatose van colon | dikke darm NNO | polypose (hereditair) van colon
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Imerslund(-Gräsbeck) syndrome Megaloblastic hereditary anaemia
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
megaloblastaire hereditaire-anemie | syndroom van Imerslund(-Gräsbeck)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : becker     bessel-hagen disease     dystrophia myotonica     imerslund syndrome megaloblastic hereditary anaemia     isaacs     myotonia congenita nos     myotonia permanens     neuromyotonia     paramyotonia congenita pseudomyotonia     steinert     thomsen     thomsen disease     congenital myotonia     dominant     drug-induced     hereditary deforming chondrodysplasia     hereditary disposition     hereditary multiple exostosis     hereditary myotonia     hereditary predisposition     medical genetics     multiple cartilaginous exostoses     multiple exostosis     multiple osteochondromas     recessive     symptomatic     Hereditary myotonia     


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Date index: 2023-03-29
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