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Translation of "Fatigue syndrome " (English → French) :
TERMINOLOGY
see also In-Context Translations below Fatigue refers to a lack of energy, and it may be either acute or chronic. Fatigue may result from exertion, stress, and a wide variety of underlying medical conditions, including infections, malignancies, autoimmune disorders, anxiety, and depressio
fatigue
SNOMEDCT-BE (finding) / 84229001
SNOMEDCT-BE (finding) / 84229001
Management of fatigue
gestion de la fatigue
SNOMEDCT-BE (regime/therapy) / 713121000
SNOMEDCT-BE (regime/therapy) / 713121000
Assessment of fatigue
évaluation de la fatigue
SNOMEDCT-BE (procedure) / 709474002
SNOMEDCT-BE (procedure) / 709474002
Malaise and fatigue
malaise et fatigue
SNOMEDCT-BE (finding) / 271795006
SNOMEDCT-BE (finding) / 271795006
A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c
leucémie aigüe myéloïde héréditaire
SNOMEDCT-BE (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c / 764940002
SNOMEDCT-BE (disorder) / 764940002
A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib
syndrome de Mœbius
SNOMEDCT-BE (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib / 89444000
SNOMEDCT-BE (disorder) / 89444000
A Noonan-related syndrome with characteristics of facial anomalies suggestive of Noonan syndrome, a distinctive hair anomaly described as loose anagen hair syndrome, frequent congenital heart defects, distinctive skin features with darkly pigmented s
syndrome Noonan-like avec cheveux anagènes caducs
SNOMEDCT-BE (disorder) / 723444009
SNOMEDCT-BE (disorder) / 723444009
Rare syndrome with the association of congenital nephrotic syndrome, ocular anomalies and microcoria. The disorder results in proteinuria with nephrotic syndrome and histological lesions marked by diffuse mesangial sclerosis. Ocular anomalies are pre
syndrome de Pierson
SNOMEDCT-BE (disorder) / 723449004
SNOMEDCT-BE (disorder) / 723449004
syndrome
syndrome | syndrome
UGENT - Medical terms -
UGENT - Medical terms -
AFG3L2 (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome
syndrome d'ataxie spastique-epilepsie myoclonique-neuropathie précoce
SNOMEDCT-BE (AFG3 like matrix AAA peptidase subunit 2) related spastic ataxia, myoclonic epilepsy, neuropathy syndrome / 771469002
SNOMEDCT-BE (disorder) / 771469002
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'Fatigue syndrome'
Date index:2023-02-19 -
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