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Translation of "other diseases " (English → French) :
TERMINOLOGY
see also In-Context Translations below 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 form of Parkinson disease with age of onset between 21 and 45 years, rigidity, painful cramps followed by tremor, bradykinesia, dystonia, gait complaints, falls and other non-motor symptoms. A slow disease progression and a more pronounced response
maladie de Parkinson à début précoce
SNOMEDCT-BE (disorder) / 715345007
SNOMEDCT-BE (disorder) / 715345007
A rare rheumatologic disease characterised by predominantly bilateral, chronic, sterile inflammation and progressive sclerosis and hyperostosis of the sternocostoclavicular joint, with adjacent soft tissue ossification, in the absence of other joint
hyperostose sterno-costo-claviculaire isolée
SNOMEDCT-BE (disorder) / 766711009
SNOMEDCT-BE (disorder) / 766711009
A rare neurologic disease with characteristics of persistent continuous bilateral visual experience of flickering snow-like dots throughout the visual field in association with other visual (including palinopsia, enhanced entopic phenomena, nyctalopi
syndrome de neige visuelle
SNOMEDCT-BE (including palinopsia, enhanced entopic phenomena, nyctalopi / 771237009
SNOMEDCT-BE (disorder) / 771237009
A rare genetic renal disease characterized by hereditary nephritis leading to nephrotic syndrome and end-stage renal failure associated with sensorineural hearing loss and pretibial skin blistering followed by atrophy. Other reported manifestations i
syndrome néphrotique-surdité-épidermolyse bulleuse prétibiale
SNOMEDCT-BE (disorder) / 773647007
SNOMEDCT-BE (disorder) / 773647007
Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo
ataxie spinocérébelleuse type 38
SNOMEDCT-BE (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo / 734021001
SNOMEDCT-BE (disorder) / 734021001
Care given to improve the quality of life of patients who have a serious or life-threatening disease. The goal of symptom management is to prevent or treat as early as possible the symptoms of a disease, side effects caused by treatment of a disease,
gestion des symptômes
SNOMEDCT-BE (procedure) / 713148004
SNOMEDCT-BE (procedure) / 713148004
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
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 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
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'other diseases'
Date index:2023-10-03 -
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