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Descriptor English: Parkinsonian Disorders
Descriptor Spanish: Trastornos Parkinsonianos
Descriptor trastornos parkinsonianos
Entry term(s) parkinsonismo
parkinsonismo autosómico dominante
parkinsonismo autosómico recesivo
parkinsonismo experimental
parkinsonismo juvenil
parkinsonismo juvenil autosómico dominante
parkinsonismo juvenil autosómico recesivo
parkinsonismo juvenil familiar
síndrome de parálisis de Ramsay Hunt
síndrome parkinsoniano
Scope note: Grupo de enfermedades con trastornos del control motor caracterizadas por bradicinesia, RIGIDEZ MUSCULAR, TEMBLOR e inestabilidad postural. Las enfermedades parkinsonianas se dividen generalmente en parkinsonismo primario (ver ENFERMEDAD DE PARKINSON), parkinsonismo secundario (ver ENFERMEDAD DE PARKINSON SECUNDARIA) y formas heredadas. Estas afecciones se asocian con disfunción de las vías dopaminérgicas o relacionadas con ellas que intervienen en la integración neuronal motora en los GANGLIOS BASALES.
Descriptor Portuguese: Transtornos Parkinsonianos
Descriptor French: Syndromes parkinsoniens
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
Chromosome 6-Linked Autosomal Recessive Parkinsonism
Diseases, Experimental Parkinson
Dominant Parkinsonism, Autosomal
Experimental Parkinson Disease
Experimental Parkinson Diseases
Experimental Parkinsonism
Experimental Parkinsonism, MPTP Induced
Experimental Parkinsonism, MPTP-Induced
Experimental Parkinsonisms
Familial Juvenile Parkinsonism
Familial Parkinson Disease, Autosomal Recessive
Juvenile Parkinson Disease
Juvenile Parkinson Disease, Autosomal Dominant
Juvenile Parkinson Disease, Autosomal Recessive
Juvenile Parkinsonism
Juvenile Parkinsonism, Autosomal Dominant
Juvenile Parkinsonism, Autosomal Recessive
Juvenile Parkinsonism, Familial
Juvenile Parkinsonisms
MPTP Induced Experimental Parkinsonism
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
Parkinson Diseases, Experimental
Parkinsonian Diseases
Parkinsonian Syndrome
Parkinsonian Syndromes
Parkinsonism
Parkinsonism, Autosomal Dominant
Parkinsonism, Autosomal Recessive
Parkinsonism, Early Onset, with Diurnal Fluctuation
Parkinsonism, Early-Onset, With Diurnal Fluctuation
Parkinsonism, Experimental
Parkinsonism, Familial Juvenile
Parkinsonism, Juvenile
Parkinsonism, Juvenile, Autosomal Dominant
Parkinsonism, Juvenile, Autosomal Recessive
Parkinsonism, MPTP-Induced Experimental
Parkinsonisms, Experimental
Parkinsonisms, Juvenile
Ramsay Hunt Paralysis Syndrome
Recessive Parkinsonism, Autosomal
Tree number(s): C10.228.140.079.862
C10.228.662.600
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D020734
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.
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
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Parkinson Disease (1966-1999)
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
Entry Version: PARKINSONIAN DIS
Related: Striatonigral Degeneration MeSH
DeCS ID: 34223
Unique ID: D020734
NLM Classification: WL 359
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2000/01/01
Date of Entry: 1999/11/08
Revision Date: 2019/07/05
Parkinsonian Disorders - Preferred
Concept UI M0328250
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.
Preferred term Parkinsonian Disorders
Entry term(s) Parkinsonian Diseases
Parkinsonian Syndrome
Parkinsonian Syndromes
Parkinsonism
Autosomal Dominant Parkinsonism - Narrower
Concept UI M0335827
Preferred term Autosomal Dominant Parkinsonism
Entry term(s) Dominant Parkinsonism, Autosomal
Parkinsonism, Autosomal Dominant
Autosomal Recessive Juvenile Parkinson Disease - Narrower
Concept UI M0332913
Preferred term Autosomal Recessive Juvenile Parkinson Disease
Entry term(s) Autosomal Recessive Juvenile Parkinsonism
Chromosome 6 Linked Autosomal Recessive Parkinsonism
Chromosome 6-Linked Autosomal Recessive Parkinsonism
Familial Parkinson Disease, Autosomal Recessive
Juvenile Parkinson Disease, Autosomal Recessive
Juvenile Parkinsonism, Autosomal Recessive
Parkinson Disease 2
Parkinson Disease 2, Autosomal Recessive Juvenile
Parkinson Disease Autosomal Recessive, Early Onset
Parkinson Disease, Familial, Autosomal Recessive
Parkinson Disease, Juvenile, Autosomal Recessive
Parkinsonism, Early Onset, with Diurnal Fluctuation
Parkinsonism, Early-Onset, With Diurnal Fluctuation
Parkinsonism, Juvenile, Autosomal Recessive
Ramsay Hunt Paralysis Syndrome - Related but not broader or narrower
Concept UI M0015966
Preferred term Ramsay Hunt Paralysis Syndrome
Familial Juvenile Parkinsonism - Narrower
Concept UI M0335826
Preferred term Familial Juvenile Parkinsonism
Entry term(s) Juvenile Parkinsonism, Familial
Parkinsonism, Familial Juvenile
Parkinsonism, Experimental - Narrower
Concept UI M0332504
Preferred term Parkinsonism, Experimental
Entry term(s) Diseases, Experimental Parkinson
Experimental Parkinson Disease
Experimental Parkinson Diseases
Experimental Parkinsonism
Experimental Parkinsonism, MPTP Induced
Experimental Parkinsonism, MPTP-Induced
Experimental Parkinsonisms
MPTP Induced Experimental Parkinsonism
MPTP-Induced Experimental Parkinsonism
Parkinson Disease, Experimental
Parkinson Diseases, Experimental
Parkinsonism, MPTP-Induced Experimental
Parkinsonisms, Experimental
Parkinsonism, Juvenile - Narrower
Concept UI M0332505
Preferred term Parkinsonism, Juvenile
Entry term(s) Juvenile Parkinson Disease
Juvenile Parkinsonism
Juvenile Parkinsonisms
Parkinson Disease, Juvenile
Parkinsonisms, Juvenile
Autosomal Dominant Juvenile Parkinson Disease - Narrower
Concept UI M0332503
Preferred term Autosomal Dominant Juvenile Parkinson Disease
Entry term(s) Autosomal Dominant Juvenile Parkinsonism
Juvenile Parkinson Disease, Autosomal Dominant
Juvenile Parkinsonism, Autosomal Dominant
Parkinson Disease, Autosomal Dominant. Juvenile
Parkinson Disease, Juvenile, Autosomal Dominant
Parkinsonism, Juvenile, Autosomal Dominant
Autosomal Recessive Parkinsonism - Narrower
Concept UI M0335828
Preferred term Autosomal Recessive Parkinsonism
Entry term(s) Parkinsonism, Autosomal Recessive
Recessive Parkinsonism, Autosomal



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