loading...| Preferred Name |
Parkinsonian Disorders |
| Synonyms |
Experimental Parkinsonisms |
| 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 |
Experimental Parkinsonisms Parkinsonism, Familial Juvenile Parkinson Diseases, Experimental Experimental Parkinsonism, MPTP Induced Juvenile Parkinsonism, Autosomal Recessive Autosomal Dominant Parkinsonism Parkinson Disease, Familial, Autosomal Recessive Experimental Parkinson Diseases Parkinson Disease, Autosomal Dominant. Juvenile Juvenile Parkinson Disease Parkinson Disease Autosomal Recessive, Early Onset Experimental Parkinsonism, MPTP-Induced MPTP Induced Experimental Parkinsonism Familial Parkinson Disease, Autosomal Recessive Chromosome 6 Linked Autosomal Recessive Parkinsonism Autosomal Dominant Juvenile Parkinson Disease Juvenile Parkinson Disease, Autosomal Dominant Autosomal Dominant Juvenile Parkinsonism Parkinsonian Diseases Parkinson Disease, Juvenile Parkinsonism, Juvenile, Autosomal Dominant Parkinsonisms, Experimental Chromosome 6-Linked Autosomal Recessive Parkinsonism Juvenile Parkinsonisms Juvenile Parkinson Disease, Autosomal Recessive Parkinsonism, Autosomal Dominant Parkinson Disease, Experimental Parkinson Disease 2 Diseases, Experimental Parkinson Parkinson Disease, Juvenile, Autosomal Dominant Juvenile Parkinsonism, Familial Autosomal Recessive Juvenile Parkinsonism Parkinsonism, MPTP-Induced Experimental Parkinsonisms, Juvenile Parkinsonian Syndrome Parkinsonism, Early-Onset, With Diurnal Fluctuation Recessive Parkinsonism, Autosomal Parkinsonism Familial Juvenile Parkinsonism Experimental Parkinsonism Autosomal Recessive Parkinsonism Parkinsonism, Juvenile, Autosomal Recessive Autosomal Recessive Juvenile Parkinson Disease Parkinsonian Syndromes Parkinsonism, Early Onset, with Diurnal Fluctuation Parkinson Disease 2, Autosomal Recessive Juvenile Juvenile Parkinsonism, Autosomal Dominant Ramsay Hunt Paralysis Syndrome Parkinsonism, Juvenile Juvenile Parkinsonism Dominant Parkinsonism, Autosomal Parkinsonism, Experimental MPTP-Induced Experimental Parkinsonism Parkinsonism, Autosomal Recessive Experimental Parkinson Disease Parkinson Disease, Juvenile, Autosomal Recessive |
| 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 |
C0752097 C0752100 C0752098 C0752104 C1868675 C0752101 C0242422 C0242423 C0752105 |
| 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/Q000401 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000523 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000652 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000151 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000209 |
| 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/C537177 http://purl.bioontology.org/ontology/MESH/C564631 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 |
T364465 T364473 T369848 T000956602 T030433 T364474 T369853 T834108 T364472 T364459 T834106 T364478 T369851 T364464 T030425 T369855 T364477 T834105 T369847 T369857 T364468 T364471 T363707 T358250 T364467 T809230 T834107 T369856 T364429 T030424 T363706 T364475 T809232 T369854 T369852 T369850 T363708 T364466 T364476 |
| TH |
UNK (19XX) NLM (1992) NLM (2000) ORD (2010) OMIM (2013) NLM (2020) |
| tui |
T050 T047 |
| subClassOf |