| Dataset | PhosphoSitePlus Phosphosite-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A neurodegenerative disease and an autosomal dominant disease that 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. (Human Disease Ontology, DOID_12858) |
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2 proteins associated with the disease Huntington's disease from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.