Medical Subject Headings

Last uploaded: January 31, 2024
Preferred Name

Parkinsonian Disorders

Synonyms

Parkinson Disease, Experimental

Autosomal Dominant Parkinsonism

Definitions

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.

ID

http://purl.bioontology.org/ontology/MESH/D020734

altLabel

Parkinson Disease, Experimental

Experimental Parkinson Disease

Parkinson Disease Autosomal Recessive, Early Onset

Chromosome 6 Linked Autosomal Recessive Parkinsonism

Juvenile Parkinson Disease

Parkinson Disease 2, Autosomal Recessive Juvenile

Familial Juvenile Parkinsonism

Parkinsonism, MPTP-Induced Experimental

Autosomal Recessive Parkinsonism

Parkinsonism, Autosomal Dominant

Juvenile Parkinsonisms

Parkinson Disease, Juvenile, Autosomal Recessive

Experimental Parkinson Diseases

Parkinsonism

Parkinsonisms, Experimental

Familial Parkinson Disease, Autosomal Recessive

Parkinson Disease, Autosomal Dominant. Juvenile

Parkinson Disease, Juvenile, Autosomal Dominant

Autosomal Recessive Juvenile Parkinson Disease

Experimental Parkinsonism, MPTP-Induced

Parkinsonism, Juvenile, Autosomal Recessive

Parkinson Disease, Juvenile

Diseases, Experimental Parkinson

Autosomal Dominant Juvenile Parkinson Disease

Parkinsonism, Early-Onset, With Diurnal Fluctuation

Parkinsonism, Familial Juvenile

Parkinsonism, Experimental

Ramsay Hunt Paralysis Syndrome

Parkinson Diseases, Experimental

Juvenile Parkinsonism, Autosomal Recessive

Dominant Parkinsonism, Autosomal

MPTP-Induced Experimental Parkinsonism

Parkinson Disease 2

Parkinson Disease, Familial, Autosomal Recessive

Parkinsonian Diseases

Juvenile Parkinsonism

Parkinsonism, Juvenile

Juvenile Parkinson Disease, Autosomal Dominant

Parkinsonian Syndromes

Juvenile Parkinsonism, Autosomal Dominant

Experimental Parkinsonisms

Autosomal Dominant Juvenile Parkinsonism

Juvenile Parkinsonism, Familial

Experimental Parkinsonism, MPTP Induced

Autosomal Recessive Juvenile Parkinsonism

Parkinsonisms, Juvenile

Experimental Parkinsonism

Parkinsonism, Autosomal Recessive

Parkinsonism, Juvenile, Autosomal Dominant

Juvenile Parkinson Disease, Autosomal Recessive

Parkinsonism, Early Onset, with Diurnal Fluctuation

Parkinsonian Syndrome

Recessive Parkinsonism, Autosomal

Chromosome 6-Linked Autosomal Recessive Parkinsonism

MPTP Induced Experimental Parkinsonism

Autosomal Dominant Parkinsonism

AN

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

AQL

BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI

cui

C0752104

C0242422

C0242423

C0752105

C0752098

C0752097

C1868675

C0752100

C0752101

DC

1

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.

DX

20000101

FX

D020955

HN

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

Inverse of AQ

http://purl.bioontology.org/ontology/MESH/Q000097

http://purl.bioontology.org/ontology/MESH/Q000178

http://purl.bioontology.org/ontology/MESH/Q000175

http://purl.bioontology.org/ontology/MESH/Q000628

http://purl.bioontology.org/ontology/MESH/Q000276

http://purl.bioontology.org/ontology/MESH/Q000134

http://purl.bioontology.org/ontology/MESH/Q000139

http://purl.bioontology.org/ontology/MESH/Q000266

http://purl.bioontology.org/ontology/MESH/Q000378

http://purl.bioontology.org/ontology/MESH/Q000517

http://purl.bioontology.org/ontology/MESH/Q000662

http://purl.bioontology.org/ontology/MESH/Q000469

http://purl.bioontology.org/ontology/MESH/Q000151

http://purl.bioontology.org/ontology/MESH/Q000150

http://purl.bioontology.org/ontology/MESH/Q000821

http://purl.bioontology.org/ontology/MESH/Q000191

http://purl.bioontology.org/ontology/MESH/Q000196

http://purl.bioontology.org/ontology/MESH/Q000473

http://purl.bioontology.org/ontology/MESH/Q000145

http://purl.bioontology.org/ontology/MESH/Q000382

http://purl.bioontology.org/ontology/MESH/Q000451

http://purl.bioontology.org/ontology/MESH/Q000453

http://purl.bioontology.org/ontology/MESH/Q000534

http://purl.bioontology.org/ontology/MESH/Q000532

http://purl.bioontology.org/ontology/MESH/Q000503

http://purl.bioontology.org/ontology/MESH/Q000188

http://purl.bioontology.org/ontology/MESH/Q000235

http://purl.bioontology.org/ontology/MESH/Q000201

http://purl.bioontology.org/ontology/MESH/Q000209

http://purl.bioontology.org/ontology/MESH/Q000208

http://purl.bioontology.org/ontology/MESH/Q000601

http://purl.bioontology.org/ontology/MESH/Q000000981

http://purl.bioontology.org/ontology/MESH/Q000652

http://purl.bioontology.org/ontology/MESH/Q000523

http://purl.bioontology.org/ontology/MESH/Q000401

Inverse of RO

http://purl.bioontology.org/ontology/MESH/D020955

Machine permutation

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

Mapped from

http://purl.bioontology.org/ontology/MESH/C566017

http://purl.bioontology.org/ontology/MESH/C567844

http://purl.bioontology.org/ontology/MESH/C537177

http://purl.bioontology.org/ontology/MESH/C566822

http://purl.bioontology.org/ontology/MESH/C564631

http://purl.bioontology.org/ontology/MESH/C565115

MDA

19991108

MMR

20190705

MN

C10.228.140.079.862

C10.228.662.600

notation

D020734

prefLabel

Parkinsonian Disorders

TERMUI

T369855

T369852

T364477

T364465

T364429

T363707

T369857

T364475

T834107

T364472

T364467

T364466

T364471

T364459

T030433

T834105

T363708

T358250

T364473

T809230

T364478

T000956602

T369851

T834108

T364464

T369847

T809232

T363706

T369853

T364468

T030424

T364474

T364476

T369848

T369850

T369856

T834106

T030425

T369854

TH

OMIM (2013)

NLM (2000)

NLM (2020)

NLM (1992)

UNK (19XX)

ORD (2010)

tui

T047

T050

subClassOf

http://purl.bioontology.org/ontology/MESH/D009069

http://purl.bioontology.org/ontology/MESH/D001480

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MSHFRE/D020734 MSHFRE CUI
http://purl.bioontology.org/ontology/ICD10CM/G20.C ICD10CM CUI
http://purl.bioontology.org/ontology/MSHFRE/D020734 MSHFRE CUI
http://purl.bioontology.org/ontology/RCD/X003a RCD CUI
http://purl.bioontology.org/ontology/MSHFRE/D020734 MSHFRE CUI
http://purl.bioontology.org/ontology/MSHFRE/D020734 MSHFRE CUI
http://purl.bioontology.org/ontology/OMIM/602544 OMIM CUI
http://purl.bioontology.org/ontology/MSHFRE/D020734 MSHFRE CUI
http://purl.bioontology.org/ontology/MSHFRE/D020734 MSHFRE CUI
http://purl.bioontology.org/ontology/SNOMEDCT/32798002 SNOMEDCT CUI
http://purl.bioontology.org/ontology/MDRGER/10073684 MDRGER CUI
http://purl.bioontology.org/ontology/SNMI/DA-21010 SNMI CUI
http://purl.bioontology.org/ontology/ICPC2P/N87003 ICPC2P CUI
http://purl.bioontology.org/ontology/MDRFRE/10034010 MDRFRE CUI
http://purl.bioontology.org/ontology/MSHFRE/D020734 MSHFRE CUI
http://purl.bioontology.org/ontology/WHOFRE/0106 WHOFRE CUI
http://purl.bioontology.org/ontology/MEDDRA/10073684 MEDDRA CUI
http://purl.bioontology.org/ontology/MDRFRE/10073684 MDRFRE CUI
http://purl.bioontology.org/ontology/SCTSPA/32798002 SCTSPA CUI
http://purl.bioontology.org/ontology/MDRGER/10034010 MDRGER CUI
http://purl.bioontology.org/ontology/CST/EXTRAPYR%20SYND COSTART CUI
http://purl.bioontology.org/ontology/MEDDRA/10034010 MEDDRA CUI
http://purl.bioontology.org/ontology/OMIM/MTHU000764 OMIM CUI
http://purl.bioontology.org/ontology/RCD/X003Z RCD CUI
http://purl.bioontology.org/ontology/NDFRT/N0000004168 NDFRT CUI
http://purl.bioontology.org/ontology/phenX/130100 PHENX CUI
http://purl.bioontology.org/ontology/OMIM/MTHU003921 OMIM CUI
http://purl.bioontology.org/ontology/WHO/0106 WHO-ART CUI
http://purl.bioontology.org/ontology/MSHFRE/D020734 MSHFRE CUI
http://purl.bioontology.org/ontology/SNOMEDCT/230291001 SNOMEDCT CUI
http://purl.bioontology.org/ontology/SCTSPA/230291001 SCTSPA CUI
http://purl.bioontology.org/ontology/MSHFRE/D020734 MSHFRE CUI
http://purl.bioontology.org/ontology/OMIM/600116 OMIM CUI
http://doe-generated-ontology.com/OntoAD#C0242422 ONTOAD LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#24819 OCHV LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.662.600 RH-MESH LOOM
http://www.semanticweb.org/ftuha/ontologies/2021/5/FRMO-01untitled-ontology-175/Parkinsonian_Disorders FRMO LOOM
http://purl.obolibrary.org/obo/OMIT_0020583 OMIT LOOM
http://purl.jp/bio/4/id/200906036886513691 IOBC LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.079.862 RH-MESH LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038307 PMAPP-PMO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D020734 RH-MESH LOOM