A very rare genetic vascular disease of autosomal recessive inheritance, described in less than 20 patients to date. The disease has manifestations of adult-onset (as early as the second decade of life) isolated calcification of the arteries of the l

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

syndrome héréditaire de calcification artérielle et articulaire

SNOMEDCT-BE (as early as the second decade of life) isolated calcification of the arteries of the l / 718602007

SNOMEDCT-BE (disorder) / 718602007

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

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

Syndrome with the association of omphalocele and cleft palate. It has been described in three daughters of normal unrelated parents. They were all diagnosed at birth. This syndrome is likely to be inherited as an autosomal recessive condition.

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

syndrome de Czeizel

SNOMEDCT-BE (disorder) / 719408007

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

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

autosomal dominant inheritance

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

transmission autosomique dominante

Viral Diseases

Maladies virales

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]

autosomal dominant inheritance

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

mode de transmission autosomique dominant | hérédité dominante | hérédité dominante autosomique | transmission autosomique dominante

biologie > génétique

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

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

SCAR2 (spinocerebellar ataxia autosomal recessive 2)

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

ataxie cérébelleuse autosomique récessive type 3

SNOMEDCT-BE (spinocerebellar ataxia autosomal recessive 2) / 715369006

SNOMEDCT-BE (disorder) / 715369006

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

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

Morvan's disease Nelaton's syndrome Sensory neuropathy:dominantly inherited | recessively inherited

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Maladie de Morvan Neuropathie sensitive héréditaire à transmission:dominante | récessive | Syndrome de Nélaton

WORLD HEALTH ORGANIZATION ICD-10: G60.8

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

autosomal recessive disorder

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

maladie héréditaire récessive autosomique | maladie autosomique récessive | maladie récessive autosomique

médecine > sémiologie et pathologie | biologie > génétique

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

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

Early-onset cerebellar ataxia with:essential tremor | myoclonus [Hunt's ataxia] | retained tendon reflexes | Friedreich's ataxia (autosomal recessive) X-linked recessive spinocerebellar ataxia

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Ataxie (de):cérébelleuse précoce avec:myoclonies [Ramsay-Hunt] | persistance des réflexes tendineux | tremblement essentiel | Friedreich (autosomique récessive) | spino-cérébelleuse récessive liée au chromosome X

WORLD HEALTH ORGANIZATION ICD-10: G11.1

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Autosomal recessive agammaglobulinaemia (Swiss type) X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency)

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Agammaglobulinémie:autosomique récessive (type suisse) | liée au chromosome X [Bruton] (avec déficit de l'hormone de croissance)

WORLD HEALTH ORGANIZATION ICD-10: D80.0

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

IN-CONTEXT TRANSLATIONS

genetic screening for autosomal recessive genes known to be prevalent, according to international scientific evidence, in the donor’s ethnic background and an assessment of the risk of transmission of inherited conditions known to be present in the family must be carried out, after consent is obtained.

https://eur-lex.europa.eu/lega (...) (...) [HTML] [2006-02-07]

Le dépistage génétique des gènes récessifs autosomiques prévalents dans le contexte ethnique du donneur selon les connaissances scientifiques internationales et l’évaluation du risque de transmission des facteurs héréditaires présents dans la famille doivent être effectués avec l'accord du donneur.

https://eur-lex.europa.eu/lega (...) (...) [HTML] [2006-02-07]

https://eur-lex.europa.eu/lega (...) [HTML] [2006-02-07]

http://eur-lex.europa.eu/legal (...) (...) [HTML] [2005-12-31]

http://eur-lex.europa.eu/legal (...) [HTML] [2005-12-31]

Others have searched : bruton hunt's ataxia autosomal dominant inheritance autosomal recessive disorder autosomal recessive inheritance myoclonus recessively inherited retained tendon reflexes

www.wordscope.com (v4.0.br.77)

'autosomal recessive inheritance'

Date index:2022-11-10 -

Pour agences de traduction et traducteurs - For translation agencies & translators

Paris - Brussels - Montreal - Genève - Luxembourg - Madrid

Wordscope - Professional computer-assisted translation tools (CAT tools)

Translation of "autosomal recessive inheritance " (English → French) :

Pour agences de traduction et traducteurs - For translation agencies & translators Paris - Brussels - Montreal - Genève - Luxembourg - Madrid Wordscope - Professional computer-assisted translation tools (CAT tools)

Pour agences de traduction et traducteurs - For translation agencies & translators

Paris - Brussels - Montreal - Genève - Luxembourg - Madrid

Wordscope - Professional computer-assisted translation tools (CAT tools)