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WormBase Tree Display for DO_term: DOID:12858

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Name Class

DOID:12858NameHuntington's disease
StatusValid
DefinitionA neurodegenerative disease that has_material_basis_in autosomal dominant inheritance and is characterized by unwanted choreatic movements, behavioral and psychiatric disturbances and dementia and has_material_basis_in expansion of CAG triplet repeats (glutamine) resulting in neuron degeneration affecting muscle coordination, cognitive abilities.
SynonymExactHD
Huntington disease
Huntington's chorea
ParentIs_aDOID:1289
DB_infoDatabaseOMIMdisease143100
Disease_model_annotationWBDOannot00000172
WBDOannot00000173
WBDOannot00000281
WBDOannot00000618
WBDOannot00000619
WBDOannot00000861
WBDOannot00000864
WBDOannot00000865
WBDOannot00000866
WBDOannot00000867
WBDOannot00000981
WBDOannot00000984
WBDOannot00000985
WBDOannot00000988
WBDOannot00000989
WBDOannot00000996
WBDOannot00000997
WBDOannot00001050
WBDOannot00001269
WBDOannot00001315
WBDOannot00001341
WBDOannot00001342
WBDOannot00001363
WBDOannot00001364
Attribute_ofGene_by_biologyWBGene00018294
WBGene00000474
WBGene00000473
WBGene00018467
Gene_by_orthology (56)
Disease_modifier_geneWBGene00021934
Disease_model_variationWBVar00092875
Disease_modifier_variationWBVar00241632
Disease_model_strainWBStrain00000182
WBStrain00000183
WBStrain00008294
WBStrain00048295
WBStrain00048293
WBStrain00048296
WBStrain00048846
WBStrain00048847
WBStrain00048848
WBStrain00050412
WBStrain00050414
Disease_model_transgeneWBTransgene00001975
Disease_model_genotypeWBGenotype00000027
WBGenotype00000068
Molecule_modifierWBMol:00005124
WBMol:00002745
WBMol:00007948
WBMol:00007949
WBMol:00007970