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WormBase Tree Display for DO_term: DOID:14330

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Name Class

DOID:14330NameParkinson's disease
StatusValid
DefinitionA synucleinopathy that has_material_basis_in degeneration of the central nervous system that often impairs motor skills, speech, and other functions.
CommentXref MGI.
SynonymExactParkinson disease
paralysis agitans
ParentIs_aDOID:0050890
ChildIsDOID:0060892
DOID:0060894
Disease_model_annotation (114)
Attribute_ofGene_by_biology (49)
Gene_by_orthologyWBGene00000018
WBGene00000035
WBGene00000037
WBGene00000038
WBGene00000102
WBGene00000103
WBGene00000138
WBGene00000227
WBGene00000239
WBGene00000295
WBGene00000296
WBGene00000417
WBGene00000418
WBGene00000439
WBGene00000819
WBGene00000898
WBGene00000908
WBGene00001043
WBGene00001052
WBGene00001053
WBGene00001708
WBGene00001749
WBGene00001758
WBGene00001771
WBGene00001773
WBGene00001789
WBGene00001792
WBGene00001975
WBGene00002005
WBGene00002010
WBGene00002299
WBGene00002363
WBGene00003587
WBGene00003589
WBGene00003605
WBGene00003607
WBGene00003638
WBGene00003967
WBGene00004049
WBGene00004212
WBGene00004374
WBGene00004378
WBGene00004876
WBGene00004877
WBGene00004878
WBGene00004930
WBGene00006510
WBGene00006514
WBGene00006541
WBGene00006562
WBGene00006721
WBGene00006722
WBGene00006723
WBGene00006763
WBGene00006793
WBGene00006795
WBGene00006933
WBGene00007036
WBGene00008706
WBGene00009027
WBGene00009174
WBGene00009278
WBGene00009992
WBGene00011936
WBGene00012084
WBGene00012319
WBGene00012586
WBGene00013094
WBGene00013258
WBGene00013260
WBGene00015184
WBGene00015337
WBGene00015391
WBGene00015467
WBGene00016002
WBGene00016204
WBGene00016392
WBGene00016393
WBGene00016661
WBGene00016789
WBGene00017137
WBGene00017268
WBGene00018911
WBGene00018912
WBGene00019636
WBGene00019900
WBGene00020506
WBGene00020909
WBGene00021009
WBGene00021160
WBGene00021566
WBGene00022010
WBGene00043097
Disease_modifier_geneWBGene00019327
Disease_model_variation (13)
Disease_modifier_variationWBVar00145463
WBVar00088288
WBVar00088251
WBVar00092006
WBVar00092244
WBVar00145666
WBVar00239446
Disease_model_strain (13)
Disease_model_transgeneWBTransgene00005869
WBTransgene00005871
WBTransgene00005873
WBTransgene00005874
WBTransgene00005875
Disease_model_genotypeWBGenotype00000032
WBGenotype00000033
WBGenotype00000031
WBGenotype00000107
WBGenotype00000146
WBGenotype00000147
Chemical_inducerWBMol:00004565
WBMol:00002747
WBMol:00004908
WBMol:00004310
WBMol:00005087
WBMol:00004258
WBMol:00003011
Molecule_modifier (18)