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Hereditary familial hypogonadism
Hypergonadotrophic hypogonadism
Hypergonadotropic hypogonadism
Hypogonadism
Hypogonadism with anosmia
Hypogonadotrophic hypogonadism
Hypogonadotropic hypogenitalism
Hypogonadotropic hypogonadism
Kallmann syndrome
Kallmann's syndrome
Olfactory genital dysplasia
Primary hypogonadism
Reifenstein's syndrome
Secondary hypogenitalism
Secondary hypogonadism

Translation of "hypogonadism " (English → French) :

primary hypogonadism | hypergonadotropic hypogonadism

hypogonadisme hypergonadotrophique | hypogonadisme primaire | hypogonadisme primitif
médecine
médecine


hypogonadism

hypogonadisme
médecine > physiopathologie
médecine > physiopathologie


hypogonadotrophic hypogonadism | secondary hypogonadism

hypogonadisme hypogonadotrophique | hypogonadisme secondaire
IATE - Health
IATE - Health


hypogonadotropic hypogenitalism | hypogonadotropic hypogonadism | secondary hypogenitalism | secondary hypogonadism

hypogénitalisme hypogonadotrophique | hypogénitalisme secondaire | hypogonadisme hypogonadotrophique | hypogonadisme secondaire
IATE - Health
IATE - Health


hypergonadotrophic hypogonadism | primary hypogonadism

hypergonadisme hypergonadotrophique | hypergonadisme primitif
IATE - Health
IATE - Health


A very rare syndrome with characteristics of the association of Mobius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic.

syndrome de Moebius-neuropathie axonale-hypogonadisme hypogonadotrope
SNOMEDCT-BE (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic. / 724174003
SNOMEDCT-BE (disorder) / 724174003


This syndrome has characteristics of the association of total alopecia (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism. It has been described in two brothers born to non consanguineous parents of Caucasian origin. Ele

syndrome d'alopécie-déficience intellectuelle-hypogonadisme hypergonadotrope
SNOMEDCT-BE (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism. It has been described in two brothers born to non consanguineous parents of Caucasian origin. Ele / 720981000
SNOMEDCT-BE (disorder) / 720981000


Kallmann's syndrome [ hypogonadism with anosmia | Kallmann syndrome | olfactory genital dysplasia ]

dysplasie olfactogénitale [ syndrome de Morsier-Kallmann | dysplasie olfacto-génitale | syndrome de Morsier ]
The Genitals
Organes génitaux


Reifenstein's syndrome | hereditary familial hypogonadism

syndrome de Reifenstein | hypoilial héréditaire
biologie > cytogénétique | biologie > embryologie | médecine > sémiologie et pathologie
biologie > cytogénétique | biologie > embryologie | médecine > sémiologie et pathologie


Moyamoya disease, short stature, facial dysmorphism, hypergonadotropic hypogonadism

syndrome d'angiopathie de Moyamoya-petite taille-dysmorphie faciale-hypogonadisme hypergonadotrope
SNOMEDCT-BE (disorder) / 724097003
SNOMEDCT-BE (disorder) / 724097003




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'hypogonadism'

Date index:2023-09-08 -

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