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]

syndrome héréditaire de prédisposition au cancer de l'ovaire

SNOMEDCT-BE (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec / 771080008

SNOMEDCT-BE (disorder) / 771080008

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Describes a rare group of immunodeficiencies due to specific mutations in the inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma (IKBKG) or the cytochrome b-245, beta polypeptide (CYBB) genes. The clinical manifestation is my

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

prédisposition mendélienne liée à l'X aux infections mycobactériennes

SNOMEDCT-BE (IKBKG) or the cytochrome b-245, beta polypeptide (CYBB) genes. The clinical manifestation is my / 719814009

SNOMEDCT-BE (disorder) / 719814009

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

mutation | gene mutation | genetic mutation

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

mutation | mutation génétique

biologie > génétique | biologie > génie génétique

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

base pair substitution | gene point mutation | point mutation | substitution mutation

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

mutation génique ponctuelle | mutation ponctuelle

IATE - Natural and applied sciences

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

mutator | mutator gene

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

gène mutateur | mutateur

biologie > biologie moléculaire | biologie > génétique

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

A rare familial skeletal dysplasia with characteristics of multiple epiphyseal dysplasia with extremely retarded ossification. It has been described in 6 members of a unique consanguineous family. A mutation in PTHR1 gene is responsible for this synd

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syndrome d'Eiken

SNOMEDCT-BE (disorder) / 720863002

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Others have searched : prp gene base pair substitution gene mutation gene point mutation genetic mutation mutated prp gene mutated prion protein gene mutation mutator mutator gene point mutation prion protein gene substitution mutation Mutated PrP gene

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'Mutated PrP gene'

Date index:2023-01-03 -

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Translation of "Mutated PrP gene " (English → French) :

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