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Parkinsonian Disorders
Hierarchy: | ∟ ∟ ∟ ∟ ∟ Parkinsonian Disorders 16 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ Parkinsonian Disorders 16 coordinate concepts3 subordinate concepts∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ ∟ |
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Annotation: | Gen: prefer specifics; do not confuse X ref RAMSAY HUNT PARALYSIS SYNDROME with RAMSAY HUNT AURICULAR SYNDROME see HERPES ZOSTER OTICUS or RAMSAY HUNT CEREBELLAR SYNDROME see MYOCLONIC CEREBELLAR DYSSYNERGIA
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History note: | Parkinson Disease (1966-1999)X |
historyNote*: | 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
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publicMeSHNote*: | 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
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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.
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activeMeSHYear*: | |
dateCreated*: | 1999-11-08X |
dateEstablished*: | 2000-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | lktX |
recordOriginator*: | KEVX |
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Labels and equivalent concepts: | Parkinsonismit (fi) XParkinsonismi (fi, replaced) Parkinsonism (sv) Parkinson Disease, Juvenile, Autosomal Dominant (en, replaced) Parkinsonian Diseases (en, replaced) Parkinson Disease, Juvenile (en, replaced) Parkinson Disease, Familial, Autosomal Recessive (en, replaced) Parkinson Disease, Experimental (en, replaced) Parkinsonian Syndrome (en, replaced) Parkinsonian Syndromes (en, replaced) Parkinsonism, Juvenile, Autosomal Recessive (en, replaced) Parkinsonism, Juvenile, Autosomal Dominant (en, replaced) Parkinsonism (en, replaced) Parkinson Disease, Autosomal Dominant. Juvenile (en, replaced) MPTP-Induced Experimental Parkinsonism (en, replaced) Experimental Parkinsonism (en, replaced) Experimental Parkinsonism, MPTP-Induced (en, replaced) Experimental Parkinson Disease (en, replaced) Chromosome 6-Linked Autosomal Recessive Parkinsonism (en, replaced) Autosomal Recesssive Juvenile Parkinsonism (en, replaced) Familial Parkinson Disease, Autosomal Recessive (en, replaced) Juvenile Parkinson Disease (en, replaced) Juvenile Parkinsonism, Autosomal Recessive (en, replaced) Juvenile Parkinsonism, Autosomal Dominant (en, replaced) Juvenile Parkinson Disease, Autosomal Recessive (en, replaced) Juvenile Parkinson Disease, Autosomal Dominant (en, replaced) Autosomal Dominant Juvenile Parkinsonism (en, replaced) Parkinsonismus (la-FI, replaced) |
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