Huntington disease pathway - Ontology Browser

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Huntington disease pathway (PW:0000017)
539 annotations. (View Annotations)

Parent Terms

Term With Siblings

Child Terms

disease pathways related to polyQ repeats +

dentatorubral-pallidoluysian atrophy disease pathway

Huntington disease pathway

An inherited form of a neurodegenerative disease caused by an expanded polyQ (polyglutamine) tract. It mostly affects the striatum and cortex, but extends to other regions later in its development. It manifests itself in movement disorders, psychiatric abnormalities, cognitive defects, and manifold pathways are disrupted.

spinocerebellar ataxia

Synonyms
related_synonym:	KEGG:05016