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 |
|
Inverse of RO | ||
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 |
|
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 |