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Céphalée trigémino-autonomique
Hypersegmentation
Hyposegmentation
Insuffisance autonomique primaire
Leucomélanopathie héréditaire
May-Hegglin
Neuropathie héréditaire sensitive et autonomique
Neuropathie héréditaire sensitive et autonomique type 1
Paralysie faciale congénitale héréditaire isolée
Paralysie spastique infantile ascendante héréditaire
Pelger-Huët

Translation of "autonomique héréditaire " (French → English) :

TERMINOLOGY
see also In-Context Translations below
neuropathie héréditaire sensitive et autonomique
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy
SNOMEDCT-BE (disorder) / 128205005
SNOMEDCT-BE (disorder) / 128205005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique avec surdité et retard de développement
https://browser.ihtsdotools.or (...) (...) [HTML]
This syndrome has characteristics of sensory and autonomic axonal neuropathy, sensorineural hearing loss and persistent global developmental delay. It has been described in four individuals from a consanguineous Lebanese family. Onset occurred in inf
SNOMEDCT-BE (disorder) / 717826009
SNOMEDCT-BE (disorder) / 717826009
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique type 1B
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008
SNOMEDCT-BE (disorder) / 717825008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique type 1
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008
SNOMEDCT-BE (disorder) / 397734008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
céphalée trigémino-autonomique
https://browser.ihtsdotools.or (...) (...) [HTML]
Trigeminal autonomic cephalgia
SNOMEDCT-BE (disorder) / 449814007
SNOMEDCT-BE (disorder) / 449814007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
insuffisance autonomique primaire
https://browser.ihtsdotools.or (...) (...) [HTML]
Autonomic failure
SNOMEDCT-CA (trouble) / 84438001
SNOMEDCT-CA (trouble) / 84438001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Anomalie (granulation) (granulocyte) ou syndrome de:Alder | May-Hegglin | Pelger-Huët | Hypersegmentation | Hyposegmentation | leucocytaire, héréditaire | Leucomélanopathie héréditaire
https://icd.who.int/browse10/2 (...) (...) [HTML]
Anomaly (granulation)(granulocyte) or syndrome:Alder | May-Hegglin | Pelger-Huët | Hereditary:leukocytic:hypersegmentation | hyposegmentation | leukomelanopathy
WORLD HEALTH ORGANIZATION ICD-10: D72.0
WORLD HEALTH ORGANIZATION ICD-10: D72.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
paralysie spastique infantile ascendante héréditaire
https://browser.ihtsdotools.or (...) (...) [HTML]
IAHSP - infantile onset ascending hereditary spastic paralysis
SNOMEDCT-BE (disorder) / 703543005
SNOMEDCT-BE (disorder) / 703543005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire de l'adulte jeune
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
paralysie faciale congénitale héréditaire isolée
https://browser.ihtsdotools.or (...) (...) [HTML]
An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or a
SNOMEDCT-BE (disorder) / 733091002
SNOMEDCT-BE (disorder) / 733091002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
IN-CONTEXT TRANSLATIONS
Ces nouvelles connaissances sont issues d'une étude subventionnée par les IRSC et intitulée « Le transporteur axonal des vésicules synaptiques K1F1A mute en neuropathie sensitive et autonomique héréditaire de type 2 », publiée dans la revue American Journal of Human Genetics .
http://www.cihr-irsc.gc.ca/f/4 (...) (...) [HTML]
The findings were reported in a study entitled " The axonal transporter of synaptic vesicles KIF1A is mutated in hereditary sensory and autonomic neuropathy type 2" . The study was published in the American Journal of Human Genetics and was supported by a grant from CIHR.
http://www.cihr-irsc.gc.ca/f/4 (...) (...) [HTML]
http://www.cihr-irsc.gc.ca/e/4 (...) [HTML]


Others have searched : hypersegmentation    hyposegmentation    leucomélanopathie héréditaire    may-hegglin    pelger-huët    insuffisance autonomique primaire    leucocytaire héréditaire    neuropathie héréditaire sensitive et autonomique    paralysie faciale congénitale héréditaire isolée    paralysie spastique infantile ascendante héréditaire    autonomique héréditaire    


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autonomique héréditaire

Date index:2023-10-25 -

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