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Translation of "héréditaire de 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
myopathie à corps d'inclusion héréditaire type 4
A rare non-dystrophic myopathy with characteristics of slowly progressive muscular weakness and atrophy initially involving proximal lower limbs and hip girdle and later on shoulder girdle, proximal upper limbs and axial muscles. Ambulation is usuall
SNOMEDCT-BE (disorder) / 770786001
SNOMEDCT-BE (disorder) / 770786001
neuropathie motrice distale héréditaire type 1
Autosomal dominant distal juvenile spinal muscular atrophy type 1
SNOMEDCT-BE (disorder) / 770630005
SNOMEDCT-BE (disorder) / 770630005
kératodermie palmoplantaire héréditaire type Gamborg-Nielsen
Hereditary palmoplantar keratoderma Gamborg Nielsen type
SNOMEDCT-BE (disorder) / 717228004
SNOMEDCT-BE (disorder) / 717228004
dystrophie endothéliale congénitale héréditaire type I
Congenital hereditary endothelial dystrophy type 1
SNOMEDCT-BE (disorder) / 416633008
SNOMEDCT-BE (disorder) / 416633008
dystrophie endothéliale congénitale héréditaire type II
Congenital hereditary endothelial dystrophy, 2
SNOMEDCT-BE (disorder) / 417395001
SNOMEDCT-BE (disorder) / 417395001
neuropathie héréditaire sensitive et autonomique type 1B
Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008
SNOMEDCT-BE (disorder) / 717825008
neuropathie motrice distale héréditaire type Jerash
Autosomal recessive distal spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003
neuropathie sensitivomotrice héréditaire type 4
Refsum's disease
SNOMEDCT-BE (disorder) / 25362006
SNOMEDCT-BE (disorder) / 25362006
neuropathie sensitivo-motrice héréditaire type Okinawa
An autosomal dominant form of hereditary motor and sensory neuropathy with dominant proximal involvement. Manifestations include adult-onset proximal neurogenic atrophy, sensory involvement, painful muscle cramps, fasciculations, areflexia, and high
SNOMEDCT-BE (disorder) / 715665006
SNOMEDCT-BE (disorder) / 715665006
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héréditaire de type
Date index:2022-10-24 -
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