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Dementia in Huntington's disease
Huntington disease-like 2
Huntington disease-like 4
Huntington disease-like syndrome
Huntington's disease

Translation of "huntington disease-like " (English → French) :

A rare Huntington disease-like syndrome with characteristics of childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on br
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maladie de Huntington-like 3
SNOMEDCT-BE (on br / 770939009
SNOMEDCT-BE (disorder) / 770939009
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Huntington disease-like syndrome
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syndrome pseudo-Huntington
SNOMEDCT-BE (disorder) / 702376003
SNOMEDCT-BE (disorder) / 702376003
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Huntington disease-like 4
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ataxie spinocérébelleuse type 17
SNOMEDCT-BE (disorder) / 719249005
SNOMEDCT-BE (disorder) / 719249005
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Huntington disease-like 2
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maladie de Huntington-like 2
SNOMEDCT-BE (disorder) / 721228006
SNOMEDCT-BE (disorder) / 721228006
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A form of neuroacanthocytosis with clinical characteristics of a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx anti
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syndrome de McLeod
SNOMEDCT-BE (disorder) / 724172004
SNOMEDCT-BE (disorder) / 724172004
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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
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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
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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
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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
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https://browser.ihtsdotools.or (...) [HTML]
A rare genetic skin disease characterized by multiple milium-like, comedone-like lesions and skin-colored to hyperpigmented, 1 to 2 mm-sized papules, associated with hypotrichosis and palmar/plantar pits. Lesions are usually first noticed on cheeks o
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syndrome d'hamartome basaloïde folliculaire généralisé
SNOMEDCT-BE (disorder) / 766928004
SNOMEDCT-BE (disorder) / 766928004
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https://browser.ihtsdotools.or (...) [HTML]
Dementia in Huntington's disease (G10+)
https://icd.who.int/browse10/2 (...) (...) [HTML]
Démence de la maladie de Huntington (G10+)
WORLD HEALTH ORGANIZATION ICD-10: F02.2*
WORLD HEALTH ORGANIZATION ICD-10: F02.2*
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https://icd.who.int/browse10/2 (...) [HTML]
Huntington's disease
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Chorée de Huntington
WORLD HEALTH ORGANIZATION ICD-10: G10
WORLD HEALTH ORGANIZATION ICD-10: G10
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]


Others have searched : dementia in huntington's disease    huntington disease-like    huntington disease-like syndrome    huntington's disease    


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'huntington disease-like'

Date index:2021-07-28 -

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