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GRID2-related spinocerebellar ataxia

info · Genetic

An autosomal dominant cerebellar ataxia that is characterized by cognitive delay, abnormal eye movements, and hearing loss.

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Lighting up: Anterior chamber of eyeball, Anterior segment of eyeball, Posterior segment of eyeball, Suspensory ligament of eyeball

HumanAtlas is an educational atlas — not a medical device and not medical advice. See disclaimer. 3D anatomy: Z-Anatomy / BodyParts3D (CC BY-SA 4.0). Data: Disease Ontology (CC0), Human Phenotype Ontology, NLM RxNorm/RxClass, Wikipedia (CC BY-SA).