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Anémie réfractaire avec excès de blastes type 2
Céphalée trigémino-autonomique
Neuropathie héréditaire sensitive et autonomique
Neuropathie héréditaire sensitive et autonomique type 1
Virus T-lymphotrope simien de type 1
Virus T-lymphotrope simien de type 2
Virus T-lymphotrope simien de type 3
Virus spumeux simien de type 1
Virus spumeux simien de type 2

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

TERMINOLOGY
see also In-Context Translations below
neuropathie héréditaire sensitive et autonomique type 1

Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008
SNOMEDCT-BE (disorder) / 397734008


neuropathie héréditaire sensitive et autonomique type 1B

Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008
SNOMEDCT-BE (disorder) / 717825008


neuropathie héréditaire sensitive et autonomique

Hereditary sensory and autonomic neuropathy
SNOMEDCT-BE (disorder) / 128205005
SNOMEDCT-BE (disorder) / 128205005


céphalée trigémino-autonomique

Trigeminal autonomic cephalgia
SNOMEDCT-BE (disorder) / 449814007
SNOMEDCT-BE (disorder) / 449814007


virus spumeux simien de type 1

Simian foamy virus 1
SNOMEDCT-BE (organism) / 407420005
SNOMEDCT-BE (organism) / 407420005


virus spumeux simien de type 2

Simian foamy virus 2
SNOMEDCT-BE (organism) / 407421009
SNOMEDCT-BE (organism) / 407421009


virus T-lymphotrope simien de type 3

STLV-III
SNOMEDCT-BE (organism) / 90676008
SNOMEDCT-BE (organism) / 90676008


anémie réfractaire avec excès de blastes type 2

Refractory anemia with excess blasts-2
SNOMEDCT-BE (disorder) / 415284008
SNOMEDCT-BE (disorder) / 415284008


virus T-lymphotrope simien de type 1

Simian T-lymphotropic virus 1
SNOMEDCT-BE (organism) / 407427008
SNOMEDCT-BE (organism) / 407427008


virus T-lymphotrope simien de type 2

Simian T-lymphotropic virus 2
SNOMEDCT-BE (organism) / 407429006
SNOMEDCT-BE (organism) / 407429006
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 .

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.




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autonomique type

Date index:2021-04-23 -

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