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CI - Convergence insufficiency
Chronic venous insufficiency
Inadequacy
Insufficiency
Mitral insufficiency
Pulmonic insufficiency
Venous insufficiency of leg

Translation of "Insufficiency NOS " (English → French) :

TERMINOLOGY
see also In-Context Translations below
insufficiency | inadequacy

insuffisance | insuffisance
UGENT - Medical terms -
UGENT - Medical terms -


Mitral insufficiency

régurgitation de la valve mitrale
SNOMEDCT-BE (disorder) / 48724000
SNOMEDCT-BE (disorder) / 48724000


Pulmonic insufficiency

régurgitation de la valve pulmonaire
SNOMEDCT-BE (disorder) / 91434003
SNOMEDCT-BE (disorder) / 91434003


Venous insufficiency of leg

insuffisance veineuse d'une jambe
SNOMEDCT-BE (disorder) / 234050002
SNOMEDCT-BE (disorder) / 234050002


Primary immunodeficiency with natural killer cell deficiency and adrenal insufficiency

déficit immunitaire primaire avec déficit en cellules NK et insuffisance surrénale
SNOMEDCT-BE (disorder) / 724275005
SNOMEDCT-BE (disorder) / 724275005


The most common form of congenital adrenal hyperplasia, divided into 2 clinical groups simple virilising or salt wasting forms. Manifests with genital ambiguity in females and with adrenal insufficiency in both sexes. Girls present with ambiguous gen

hyperplasie congénitale des surrénales par déficit en 21-hydroxylase classique
SNOMEDCT-BE (disorder) / 717261006
SNOMEDCT-BE (disorder) / 717261006


CI - Convergence insufficiency

insuffisance de convergence
SNOMEDCT-BE (disorder) / 194131002
SNOMEDCT-BE (disorder) / 194131002


An extremely rare genetic endocrine disease with characteristics of primary adrenal insufficiency, dystrophic myopathy, hepatic steatosis, severe psychomotor delay, megalocornea, failure to thrive, chronic constipation, and terminal bladder ectasia w

adrénomyodystrophie
SNOMEDCT-BE (disorder) / 763311001
SNOMEDCT-BE (disorder) / 763311001


Larsen-like syndrome, lethal type, has characteristics of multiple joint dislocation and respiratory insufficiency due to tracheomalacia and or lung hypoplasia. It has been described in less than ten patients. Transmission is thought to be autosomal

syndrome létal de Larsen-like
SNOMEDCT-BE (disorder) / 719409004
SNOMEDCT-BE (disorder) / 719409004


Chronic venous insufficiency

insuffisance veineuse périphérique
SNOMEDCT-BE (disorder) / 20696009
SNOMEDCT-BE (disorder) / 20696009
IN-CONTEXT TRANSLATIONS


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'Insufficiency NOS'

Date index:2021-02-03 -

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