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Translation of "Hypersensitivity types " (English → French) :
TERMINOLOGY
see also In-Context Translations below hypersensitivity | over-sensitivity
hypersensibilité | hypersensibilité
UGENT - Medical terms -
UGENT - Medical terms -
Hypersensitivity condition
condition d'hypersensibilité
SNOMEDCT-BE (finding) / 473010000
SNOMEDCT-BE (finding) / 473010000
Hypersensitivity reaction
réaction d'hypersensibilité
SNOMEDCT-BE (disorder) / 421961002
SNOMEDCT-BE (disorder) / 421961002
Hypersensitive bladder
vessie hypersensible
SNOMEDCT-BE (disorder) / 236639003
SNOMEDCT-BE (disorder) / 236639003
A group of tyrosine related oculocutaneous albinism (OCA1) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS). The phenotypic spectrum seen in OCA1 i
albinisme oculo-cutané type 1
SNOMEDCT-BE (OCA1) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS). The phenotypic spectrum seen in OCA1 i / 765146000
SNOMEDCT-BE (disorder) / 765146000
Charcot-Marie-Tooth disease, type 4B2 (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso
maladie de Charcot-Marie-Tooth type 4B2
SNOMEDCT-BE (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso / 715800000
SNOMEDCT-BE (disorder) / 715800000
A rare multiple malformation syndrome with characteristics of severe intrauterine growth retardation, severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism. Severe central nervous system defects
syndrome de Neu-Laxova
SNOMEDCT-BE (collodion baby type), and facial dysmorphism. Severe central nervous system defects / 77817004
SNOMEDCT-BE (disorder) / 77817004
This syndrome has characteristics of Hirschsprung disease and absence or hypoplasia of the nails and distal phalanges of the thumbs and great toes (type D brachydactyly). It has been described in four males from one family (two brothers and two mater
syndrome de maladie de Hirschsprung-brachydactylie type D
SNOMEDCT-BE (type D brachydactyly). It has been described in four males from one family (two brothers and two mater / 721222007
SNOMEDCT-BE (disorder) / 721222007
Classical mycosis fungoides is the most common type of mycosis fungoides, a form of cutaneous T-cell lymphoma, and is characterised by slow progression from patches to more infiltrated plaques and eventually to tumours. The disease first manifests by
mycosis fongoïde classique
SNOMEDCT-BE (disorder) / 765328000
SNOMEDCT-BE (disorder) / 765328000
Omodysplasia is a rare skeletal dysplasia characterised by severe limb shortening and facial dysmorphism. Two types of omodysplasia have been described: an autosomal recessive or generalised form (also referred to as micromelic dysplasia with disloca
omodysplasie
SNOMEDCT-BE / 725164008
SNOMEDCT-BE (disorder) / 725164008
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'Hypersensitivity types'
Date index:2022-04-29 -
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