Progressive osseous heteroplasia (POH) is a rare genetic bone disorder with clinical characteristics of progressive extraskeletal bone formation presenting in early life with cutaneous ossification that progressively involves subcutaneous and then su

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

hétéroplasie osseuse progressive

SNOMEDCT-BE (POH) is a rare genetic bone disorder with clinical characteristics of progressive extraskeletal bone formation presenting in early life with cutaneous ossification that progressively involves subcutaneous and then su / 719271000

SNOMEDCT-BE (disorder) / 719271000

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

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

Spinocerebellar ataxia type 29 (SCA29) is a rare disease with main features of very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability. SCA29 presents at birth, or shortly, after with manife

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

ataxie spinocérébelleuse type 29

SNOMEDCT-BE (SCA29) is a rare disease with main features of very slowly progressive or non-progressive ataxia, dysarthria, oculomotor abnormalities and intellectual disability. SCA29 presents at birth, or shortly, after with manife / 715825009

SNOMEDCT-BE (disorder) / 715825009

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

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

progressive image | progressive picture | progressive-scan image | progressive-scan picture

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

image à balayage progressif | image progressive

IATE - Electronics and electrical engineering

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

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

A rare genetic, poly malformative syndrome with characteristics of progressive, proportionate, asymmetric segmental overgrowth (with soft tissue hypertrophy and ballooning effect) that develops and progresses rapidly in early childhood, arteriovenous

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syndrome d'hypertrophie segmentaire-lipomatose-malformation artérioveineuse-naevus épidermique

SNOMEDCT-BE (with soft tissue hypertrophy and ballooning effect) that develops and progresses rapidly in early childhood, arteriovenous / 763867001

SNOMEDCT-BE (disorder) / 763867001

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

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

chorée de Huntington | chorée héréditaire | chorée chronique | maladie de Huntington

médecine > sémiologie et pathologie | médecine > neurologie | biologie > génétique

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

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

progressive muscular dystrophy | Erb-Landouzy disease | Erb's disease | idiopathic muscular atrophy | myodystrophia

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

médecine

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

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

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

Knight's progress

Date index:2022-01-21 -

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Translation of "Knight's progress " (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

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