parkinsonian disorders

Preferred Label : parkinsonian disorders;

MeSH definition : 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.;

MeSH synonym : parkinsonism; parkinsonian syndrome; parkinsonian syndromes; parkinsonian diseases;

MeSH hyponym : autosomal dominant parkinsonism; familial juvenile parkinsonism; parkinsonism, juvenile; autosomal recessive juvenile parkinson disease; parkinsonism, experimental; autosomal recessive parkinsonism; autosomal dominant juvenile parkinson disease; Dominant Parkinsonism, Autosomal; Parkinsonism, Autosomal Dominant; 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; Parkinsonism, Early Onset, with Diurnal Fluctuation; Parkinsonism, Juvenile, Autosomal Recessive; Parkinson Disease 2, Autosomal Recessive Juvenile; Parkinsonism, Early-Onset, With Diurnal Fluctuation; Parkinson Disease, Juvenile, Autosomal Recessive; Parkinson Disease 2; Parkinson Disease Autosomal Recessive, Early Onset; Autosomal Recesssive Juvenile Parkinsonism; Parkinson Disease, Familial, Autosomal Recessive; Juvenile Parkinsonism, Familial; Parkinsonism, Familial Juvenile; Experimental Parkinsonisms; Parkinsonisms, Experimental; Parkinson Disease, Experimental; Experimental Parkinsonism, MPTP-Induced; Experimental Parkinsonism, MPTP Induced; Parkinsonism, MPTP-Induced Experimental; MPTP-Induced Experimental Parkinsonism; MPTP Induced Experimental Parkinsonism; Experimental Parkinson Disease; Diseases, Experimental Parkinson; Experimental Parkinson Diseases; Parkinson Diseases, Experimental; Experimental Parkinsonism; Juvenile Parkinsonism; Juvenile Parkinsonisms; Parkinsonisms, Juvenile; Parkinson Disease, Juvenile; Juvenile Parkinson Disease; Juvenile Parkinson Disease, Autosomal Dominant; Parkinsonism, Juvenile, Autosomal Dominant; Parkinson Disease, Autosomal Dominant. Juvenile; Parkinson Disease, Juvenile, Autosomal Dominant; Autosomal Dominant Juvenile Parkinsonism; Juvenile Parkinsonism, Autosomal Dominant; Parkinsonism, Autosomal Recessive; Recessive Parkinsonism, Autosomal; Autosomal Recessive Juvenile Parkinsonism;

Related MeSH term : ramsay hunt paralysis syndrome;

MeSH 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; 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;

Wikipedia link : https://en.wikipedia.org/wiki/Parkinsonian syndrome;

Details

Origin ID

D020734;

UMLS CUI

C0242422;

ATC code(s)
- amantadine [ATC Code]
- bromocriptine [ATC Code]
- budipine [ATC Code]
- cabergoline [ATC Code]
- monoamine oxidase b inhibitors [ATC Code]
- pergolide [ATC Code]
- piribedil [ATC Code]
- rasagiline [ATC Code]
- selegiline [ATC Code]
- tolcapone [ATC Code]
ATC code(s)
- dihydroergocryptine mesylate [ATC Code]
- dopamine agonists [ATC Code]
- melevodopa [ATC Code]
Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- congenital [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonism (disorder) [SNOMED CT concept]
- 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine induced Parkinsonism [ICD-11 More detail]
- Autosomal recessive familial Parkinson disease [ICD-11 More detail]
- Juvenile Parkinson's disease (disorder) [SNOMED CT concept]
- Parkinsonism [DO Concept]
- juvenile paralysis agitans of hunt [SNOMED Notion]
- mptp-induced parkinsonism [SNOMED Notion]
- parkinsonism [TUV Term]
- parkinsonism [TUV Concept]
CISMeF manual mappings
- parkinsonism [ICPC-2 Rubric]
Currated CISMeF NLP mapping
- PARKINSONISM [WHO-ART Included Term]
- Parkinson Disease [NCIt concept]
- Parkinson disease [ICD-11 Subcategory]
- Parkinson's disease [ICD-9 code]
- Parkinsonism [PASCAL descriptor]
- Parkinsonism [ICD-11 Category]
- Parkinsonism [HPO term]
- Parkinsonism [MedDRA Preferred Term]
- Parkinsonism (disorder) [SNOMED CT concept]
- parkinsonism [Disease (Nov.)]
- parkinsonism, nos [SNOMED Notion]
HPO term
- Parkinsonism [HPO term]
Record concept(s)
- autosomal dominant juvenile parkinson disease [MeSH concept]
- autosomal dominant parkinsonism [MeSH concept]
- autosomal recessive juvenile parkinson disease [MeSH concept]
- autosomal recessive parkinsonism [MeSH concept]
- familial juvenile parkinsonism [MeSH concept]
- parkinsonian disorders [MeSH concept]
- parkinsonism, experimental [MeSH concept]
- parkinsonism, juvenile [MeSH concept]
- ramsay hunt paralysis syndrome [MeSH concept]
Related MeSH Supplementary Concept(s)
- Dementia-Parkinsonism With Non-Alzheimer Amyloid Plaques [MeSH Supplementary Concept]
- Dystonia-Parkinsonism, Adult-Onset [MeSH Supplementary Concept]
- Kufor-Rakeb syndrome [MeSH Supplementary Concept]
- parkinson disease 5 [MeSH Supplementary Concept]
- parkinson disease 8 [MeSH Supplementary Concept]
- perry syndrome [MeSH Supplementary Concept]
See also
- striatonigral degeneration [MeSH Descriptor]
See also (suggested by CISMeF)
- antiparkinson agents [MeSH Descriptor]
See also inter- (CISMeF)
- Parkinsonism [NCIt concept]
- Parkinsonism caused by drug (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypokinetic-rigid syndrome [MedDRA LLT]
- PARKINSONISM [WHO-ART Included Term]
- Parkinsonism [MedDRA Preferred Term]
- Parkinsonism [HPO term]
- Parkinsonism [PASCAL descriptor]
- Parkinsonism [NCIt concept]
- Parkinsonism (disorder) [SNOMED CT concept]
- Rare parkinsonian disorder [ORDO Disease]
- parkinsonism [ICPC-2 Rubric]
- parkinsonism [Disease (Nov.)]
- parkinsonism, nos [SNOMED Notion]
Validated automatic mappings to BTNT
- Autosomal recessive familial Parkinson disease (disorder) [SNOMED CT concept]
- Parkinson Disease 2, Autosomal Recessive Juvenile [NCIt concept]
- Parkinson disease 2, autosomal recessive juvenile [OMIM Phenotype]
- Parkinson's disease 2 [DO Concept]
- juvenile Parkinson syndrome [Disease (Nov.)]

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