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Adult-onset dystonia parkinsonism
Atypical juvenile parkinsonism
Dementia in paralysis agitans
Idiopathic
Parkinson disease
Parkinson's disease
Parkinsonism
Primary
Vascular parkinsonism

Translation of "Parkinsonism " (English → Dutch) :

Parkinsonism | Parkinson's disease

parkinsonisme | ziekteverschijnselen met de kenmerken van de ziekte van Parkinson
UGENT - Medical terms -
UGENT - Medical terms -


Hemiparkinsonism Paralysis agitans Parkinsonism or Parkinson's disease:NOS | idiopathic | primary

hemiparkinsonisme | paralysis agitans | parkinsonisme of ziekte van Parkinson | NNO | parkinsonisme of ziekte van Parkinson | idiopathisch | parkinsonisme of ziekte van Parkinson | primair
WORLD HEALTH ORGANIZATION ICD-10: G20
WORLD HEALTH ORGANIZATION ICD-10: G20


SNOMEDCT-BE (disorder) / 32798002
SNOMEDCT-BE (disorder) / 32798002


Vascular parkinsonism

vasculair parkinsonisme
SNOMEDCT-BE (disorder) / 230296006
SNOMEDCT-BE (disorder) / 230296006


Definition: A dementia developing in the course of established Parkinson's disease. No particular distinguishing clinical features have yet been demonstrated. | Dementia in:paralysis agitans | parkinsonism

Omschrijving: Een dementie die zich ontwikkelt in het verloop van een bestaande ziekte van Parkinson. Tot nog toe zijn er geen specifieke klinische kenmerken aangetoond. | Neventerm: | dementie bij | paralysis agitans | dementie bij | parkinsonisme
WORLD HEALTH ORGANIZATION ICD-10: F02.3*
WORLD HEALTH ORGANIZATION ICD-10: F02.3*


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

ziekte van Parkinson met aanvang op jonge leeftijd
SNOMEDCT-BE (disorder) / 715345007
SNOMEDCT-BE (disorder) / 715345007


Parkinson disease

ziekte van Parkinson
SNOMEDCT-BE (disorder) / 49049000
SNOMEDCT-BE (disorder) / 49049000


Adult-onset dystonia parkinsonism

dystonie-parkinsonisme met aanvang op volwassen leeftijd
SNOMEDCT-BE (disorder) / 720466001
SNOMEDCT-BE (disorder) / 720466001


Atypical juvenile parkinsonism

atypisch juveniel parkinsonisme
SNOMEDCT-BE (disorder) / 725146001
SNOMEDCT-BE (disorder) / 725146001


A recently described syndrome with characteristics of Wolff-Parkinson-White syndrome, variable developmental delay and facial dysmorphism. Dysmorphic features include macrocephaly, hypertelorism, down-slanting palpebral fissures and microstomia. This

del(20)(p12.3)
SNOMEDCT-BE (disorder) / 719650004
SNOMEDCT-BE (20)(p12.3) / 719650004




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'Parkinsonism'

Date index:2022-09-30 -

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