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Agammaglobulinémie isolée
Anorchidie congénitale isolée
Dysplasie corticale focale isolée
Hormone de croissance
Hormone hypophysaire
Hypertrichose cervicale antérieure isolée
Isolée en gonadotrophine
Kallmann
Lorain-Lévi
Myopie isolée rare
Paralysie faciale congénitale héréditaire isolée
Polykystose hépatique isolée
Sheehan
Staturale pituitaire SAI

Translation of "isolée en gonadotrophine " (French → English) :

Cachexie hypophysaire Hypogonadisme hypogonadotrophique Insuffisance (de):hormone de croissance idiopathique | isolée en:gonadotrophine | hormone de croissance | hormone hypophysaire | staturale pituitaire SAI | Maladie de Simmonds Nécrose pituitaire (post-partum) Panhypopituitarisme Syndrome de:eunuchoïdisme fertile | Kallmann | Lorain-Lévi | Sheehan
https://icd.who.int/browse10/2 (...) (...) [HTML]
Fertile eunuch syndrome Hypogonadotropic hypogonadism Idiopathic growth hormone deficiency Isolated deficiency of:gonadotropin | growth hormone | pituitary hormone | Kallmann's syndrome Lorain-Levi short stature Necrosis of pituitary gland (postpartum) Panhypopituitarism Pituitary:cachexia | insufficiency NOS | short stature | Sheehan's syndrome Simmonds' disease
WORLD HEALTH ORGANIZATION ICD-10: E23.0
WORLD HEALTH ORGANIZATION ICD-10: E23.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
hypomagnésémie isolée autosomique dominante type Glaudemans
https://browser.ihtsdotools.or (...) (...) [HTML]
Isolated autosomal dominant hypomagnesemia Glaudemans type
SNOMEDCT-BE (disorder) / 722008003
SNOMEDCT-BE (disorder) / 722008003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
polykystose hépatique isolée
https://browser.ihtsdotools.or (...) (...) [HTML]
A genetic disorder with characteristics of the appearance of numerous cysts spread throughout the liver. Women are predominantly affected and have a larger number of cysts than affected males. Cysts are undetectable early in life and usually appear a
SNOMEDCT-BE (disorder) / 716196007
SNOMEDCT-BE (disorder) / 716196007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
paralysie faciale congénitale héréditaire isolée
https://browser.ihtsdotools.or (...) (...) [HTML]
An extremely rare neurological disorder presumed to result from maldevelopment of the facial nucleus and/or cranial nerve reported in fewer than 10 families to date. It manifests as non-progressive, isolated, unilateral or bilateral, symmetrical or a
SNOMEDCT-BE (disorder) / 733091002
SNOMEDCT-BE (disorder) / 733091002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
dysplasie corticale focale isolée
https://browser.ihtsdotools.or (...) (...) [HTML]
Isolated focal cortical dysplasia
SNOMEDCT-BE (disorder) / 766710005
SNOMEDCT-BE (disorder) / 766710005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
dysplasie ventriculaire droite arythmogène familiale isolée
https://browser.ihtsdotools.or (...) (...) [HTML]
Familial isolated arrhythmogenic right ventricular dysplasia
SNOMEDCT-BE (disorder) / 715865008
SNOMEDCT-BE (disorder) / 715865008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
myopie isolée rare
https://browser.ihtsdotools.or (...) (...) [HTML]
Rare isolated myopia
SNOMEDCT-BE (disorder) / 773771008
SNOMEDCT-BE (disorder) / 773771008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
agammaglobulinémie isolée
https://browser.ihtsdotools.or (...) (...) [HTML]
The non-syndromic form of a primary immunodeficiency disease characterized by deficient gamma globulins and associated predisposition to frequent and recurrent infections from infancy. Two forms have been described: X-linked represents approximately
SNOMEDCT-BE (disorder) / 764858009
SNOMEDCT-BE (disorder) / 764858009
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
hypertrichose cervicale antérieure isolée
https://browser.ihtsdotools.or (...) (...) [HTML]
Hairy throat syndrome
SNOMEDCT-BE (disorder) / 717963001
SNOMEDCT-BE (disorder) / 717963001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
anorchidie congénitale isolée
https://browser.ihtsdotools.or (...) (...) [HTML]
XY Gonadal agenesis syndrome
SNOMEDCT-BE (disorder) / 53599007
SNOMEDCT-BE (disorder) / 53599007
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : kallmann    lorain-lévi    sheehan    agammaglobulinémie isolée    anorchidie congénitale isolée    dysplasie corticale focale isolée    hormone de croissance    hormone hypophysaire    hypertrichose cervicale antérieure isolée    isolée en gonadotrophine    myopie isolée rare    paralysie faciale congénitale héréditaire isolée    polykystose hépatique isolée    staturale pituitaire sai    


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isolée en gonadotrophine

Date index:2021-05-07 -

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