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Translation of "other delirium " (English → French) :
TERMINOLOGY
see also In-Context Translations below delirium | being delerious
1) délire - 2) delirium tremens | 1) idée fixe et irrationnelle - 2) delirium tremens
UGENT - Medical terms -
UGENT - Medical terms -
Delirium management
gestion du délirium
SNOMEDCT-BE (regime/therapy) / 386255004
SNOMEDCT-BE (regime/therapy) / 386255004
Delirium tremens
delirium du sevrage alcoolique
SNOMEDCT-BE (disorder) / 8635005
SNOMEDCT-BE (disorder) / 8635005
SNOMEDCT-BE (disorder) / 2776000
SNOMEDCT-BE (disorder) / 2776000
A subgroup of therapy-related myeloid neoplasms (t-MN), associated with a treatment of an unrelated neoplastic or autoimmune disease with cytotoxic agents, like cyclophosphamid, platins, melphalan and others. The neoplastic cells typically harbor unb
leucémie aigüe myéloïde et syndromes myélodysplasiques liés aux agents alkylants
SNOMEDCT-BE (t-MN), associated with a treatment of an unrelated neoplastic or autoimmune disease with cytotoxic agents, like cyclophosphamid, platins, melphalan and others. The neoplastic cells typically harbor unb / 766045006
SNOMEDCT-BE (disorder) / 766045006
A rare syndromic microphthalmia disorder with characteristics of microphthalmia with coloboma (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali
syndrome de micropthalmie colobomateuse-microcéphalie-déficience intellectuelle-petite taille liée à l'X
SNOMEDCT-BE (which may involve the iris, ciliary body, choroid, retina and/or optic nerve), microcephaly, short stature and intellectual disability. Other eye abnormali / 771148008
SNOMEDCT-BE (disorder) / 771148008
Syndrome with characteristics of precocious puberty (due to Leydig cell hyperplasia), progressive spastic paraplegia and intellectual deficit. It has been described in two brothers. The fact that other family members displayed brisk reflexes and dysa
syndrome de parésie spastique-puberté précoce
SNOMEDCT-BE (due to Leydig cell hyperplasia), progressive spastic paraplegia and intellectual deficit. It has been described in two brothers. The fact that other family members displayed brisk reflexes and dysa / 732958004
SNOMEDCT-BE (disorder) / 732958004
Syndrome that is characterized by the association of multiple sclerosis with lamellar ichthyosis and hematological anomalies (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may
syndrome de sclérose en plaques-ichtyose-déficit en facteur VIII
SNOMEDCT-BE (beta thalassemia minor and a quantitative deficit of factor VIII-von Willebrand complex). Other clinical manifestations may / 733028000
SNOMEDCT-BE (disorder) / 733028000
A subgroup of therapy-related myeloid neoplasms (t-MN), associated with treatment of an unrelated neoplastic disease with cytotoxic agents, like etoposide, doxorubicin, daunorubicin and others. The neoplastic cells often show rearrangements involving
leucémie aigüe myéloïde et syndromes myélodysplasiques liés aux inhibiteurs de la topoisomérase II
SNOMEDCT-BE (t-MN), associated with treatment of an unrelated neoplastic disease with cytotoxic agents, like etoposide, doxorubicin, daunorubicin and others. The neoplastic cells often show rearrangements involving / 766046007
SNOMEDCT-BE (disorder) / 766046007
Other ethnic, other mixed orig
autre ethnie d'origine métissée autre
SNOMEDCT-CA (groupe ethnique) / 186023009
SNOMEDCT-CA (groupe ethnique) / 186023009
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'other delirium'
Date index:2024-02-15 -
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