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Parkinsonian Disorders MeSH Descriptor Data 2021


MeSH Heading
Parkinsonian Disorders
Tree Number(s)
C10.228.140.079.862
C10.228.662.600
Unique ID
D020734
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D020734
Annotation
Gen: prefer specifics; do not confuse entry term RAMSAY HUNT PARALYSIS SYNDROME with RAMSAY HUNT AURICULAR SYNDROME see HERPES ZOSTER OTICUS or RAMSAY HUNT CEREBELLAR SYNDROME see MYOCLONIC CEREBELLAR DYSSYNERGIA
Scope Note
A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA.
Entry Version
PARKINSONIAN DIS
Entry Term(s)
Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinsonism
Autosomal Dominant Parkinsonism
Autosomal Recessive Juvenile Parkinson Disease
Autosomal Recessive Juvenile Parkinsonism
Autosomal Recessive Parkinsonism
Chromosome 6-Linked Autosomal Recessive Parkinsonism
Experimental Parkinson Disease
Experimental Parkinsonism
Experimental Parkinsonism, MPTP-Induced
Familial Juvenile Parkinsonism
Familial Parkinson Disease, Autosomal Recessive
Juvenile Parkinson Disease
Juvenile Parkinson Disease, Autosomal Dominant
Juvenile Parkinson Disease, Autosomal Recessive
Juvenile Parkinsonism, Autosomal Dominant
Juvenile Parkinsonism, Autosomal Recessive
MPTP-Induced Experimental Parkinsonism
Parkinson Disease 2
Parkinson Disease 2, Autosomal Recessive Juvenile
Parkinson Disease Autosomal Recessive, Early Onset
Parkinson Disease, Autosomal Dominant. Juvenile
Parkinson Disease, Experimental
Parkinson Disease, Familial, Autosomal Recessive
Parkinson Disease, Juvenile
Parkinson Disease, Juvenile, Autosomal Dominant
Parkinson Disease, Juvenile, Autosomal Recessive
Parkinsonian Diseases
Parkinsonian Syndrome
Parkinsonian Syndromes
Parkinsonism
Parkinsonism, Early Onset, with Diurnal Fluctuation
Parkinsonism, Early-Onset, With Diurnal Fluctuation
Parkinsonism, Experimental
Parkinsonism, Juvenile
Parkinsonism, Juvenile, Autosomal Dominant
Parkinsonism, Juvenile, Autosomal Recessive
Ramsay Hunt Paralysis Syndrome
NLM Classification #
WL 359
Previous Indexing
Parkinson Disease (1966-1999)
See Also
Striatonigral Degeneration
Public MeSH Note
2000; for PARKINSONISM see PARKINSON DISEASE 1978-1999; for PARKINSONIAN SYNDROME see PARKINSON DISEASE, SECONDARY 1974-1999: for RAMSAY HUNT PARALYSIS SYNDROME see PARKINSON DISEASE 1992-1999
History Note
2000; for PARKINSONISM use PARKINSON DISEASE 1978-1999; for PARKINSONIAN SYNDROME use PARKINSON DISEASE, SECONDARY 1974-1999; for RAMSAY HUNT PARALYSIS SYNDROME use PARKINSON DISEASE 1992-1999
Date Established
2000/01/01
Date of Entry
1999/11/08
Revision Date
2019/07/05
Parkinsonian Disorders Preferred
Autosomal Dominant Parkinsonism Narrower
Autosomal Recessive Juvenile Parkinson Disease Narrower
Ramsay Hunt Paralysis Syndrome Related
Familial Juvenile Parkinsonism Narrower
Parkinsonism, Experimental Narrower
Parkinsonism, Juvenile Narrower
Autosomal Dominant Juvenile Parkinson Disease Narrower
Autosomal Recessive Parkinsonism Narrower
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