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Dysplasie épiphysaire multiple type 1
Dysplasie épiphysaire multiple type 4
Dysplasie épiphysaire multiple type 5
Dysplasie épiphysaire multiple type Al-Gazali
Dysplasie épiphysaire multiple type Beighton
Dysplasie épiphysaire multiple type Lowry
Néoplasie endocrine multiple de type 1
Néoplasie endocrinienne multiple type 2
Néoplasie endocrinienne multiple type 4

Translation of "��piphysaire multiple type " (French → English) :

Définition: Démence de la maladie d'Alzheimer survenant avant l'âge de 65 ans, évoluant assez rapidement vers une détérioration et comportant de multiples perturbations marquées des fonctions corticales supérieures. | Démence dégénérative primaire de type Alzheimer, à début présénile Démence présénile, de type Alzheimer Maladie d'Alzheimer, type 2

Definition: Dementia in Alzheimer's disease with onset before the age of 65, with a relatively rapid deteriorating course and with marked multiple disorders of the higher cortical functions. | Alzheimer's disease, type 2 Presenile dementia, Alzheimer's type Primary degenerative dementia of the Alzheimer's type, presenile onset
WORLD HEALTH ORGANIZATION ICD-10: F00.0*
WORLD HEALTH ORGANIZATION ICD-10: F00.0*


dysplasie épiphysaire multiple type 1

Polyepiphyseal dysplasia type 1
SNOMEDCT-BE (disorder) / 715673002
SNOMEDCT-BE (disorder) / 715673002


dysplasie épiphysaire multiple type 5

Polyepiphyseal dysplasia type 5
SNOMEDCT-BE (disorder) / 715674008
SNOMEDCT-BE (disorder) / 715674008


dysplasie épiphysaire multiple type 4

Autosomal recessive multiple epiphyseal dysplasia
SNOMEDCT-BE (disorder) / 715672007
SNOMEDCT-BE (disorder) / 715672007


dysplasie épiphysaire multiple type Lowry

Multiple epiphyseal dysplasia Lowry type
SNOMEDCT-BE (disorder) / 768935003
SNOMEDCT-BE (disorder) / 768935003


dysplasie épiphysaire multiple type Beighton

Multiple epiphyseal dysplasia Beighton type
SNOMEDCT-BE (disorder) / 719689005
SNOMEDCT-BE (disorder) / 719689005


néoplasie endocrine multiple de type 1

MEN, type 1
SNOMEDCT-BE (disorder) / 30664006
SNOMEDCT-BE (disorder) / 30664006


néoplasie endocrinienne multiple type 2

MEN, type 2
SNOMEDCT-BE (disorder) / 61808009
SNOMEDCT-BE (disorder) / 61808009


néoplasie endocrinienne multiple type 4

A very rare form of multiple endocrine neoplasia, an inherited cancer syndrome, with parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors. Caused by heterozygous inactivating mutations in t
SNOMEDCT-BE (disorder) / 715907003
SNOMEDCT-BE (disorder) / 715907003


dysplasie épiphysaire multiple type Al-Gazali

Multiple epiphyseal dysplasia Al-Gazali type
SNOMEDCT-BE (disorder) / 719688002
SNOMEDCT-BE (disorder) / 719688002




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��piphysaire multiple type

Date index:2022-04-15 -

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