VPS13A-related neurodegenerative disease

MONDO:0008695

A form of neuroacanthocytosis and is characterized clinically by a Huntington disease-like phenotype with progressive neurological symptoms including movement disorders, psychiatric manifestations and cognitive disturbances, and caused by a variation in the VPS13A gene.

Also known as: CHAC, Chac, Levine-Critchley syndrome, VPS13A disease, chorea-acanthocytosis, choreoacanthocytosis

180 clinical trials for this condition and its sub-types.

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