Skip to main content

Search

Search

Main Menu

Home
Clinical Information
Patient Information
How To Use This Site chevron_right
About This Site
Search Tips

Hereditary Ocular Disease: a Database of hereditary ocular disease.

Main navigation

Home
Clinical Information
Patient Information
How To Use This Site
- Clinicians
- Patients
About This Site
Search Tips

cerebellar atrophy

Short Stature, Hearing Loss, Retinitis Pigmentosa, and Distinctive Facies

Leukodystrophy, Hypomyelinating, 15

Myopathy, Mitochondrial Anomalies, and Ataxia

Neurodevelopmental Disorder, Mitochondrial, with Abnormal Movements and Lactic Acidosis

Spinocerebellar Ataxia 37

Spastic Ataxia 8, Autosomal Recessive, with Hypomyelinating Leukodystrophy

Spinocerebellar Ataxia 3

Neurodevelopmental Disorder with Progressive Microcephaly, Spasticity, and Brain Anomalies

Ataxia with Oculomotor Apraxia 3

Image

Kufor-Rakeb Syndrome

Image

Pagination

Page 1
Next page

Subscribe to cerebellar atrophy

College of Medicine
Department of Ophthalmology and Vision Science
Acknowledgements and Rights | Admin | Login

We respectfully acknowledge the University of Arizona is on the land and territories of Indigenous peoples. Today, Arizona is home to 22 federally recognized tribes, with Tucson being home to the O’odham and the Yaqui. The university strives to build sustainable relationships with sovereign Native Nations and Indigenous communities through education offerings, partnerships, and community service.

University Information Security and Privacy

© 2026 The Arizona Board of Regents on behalf of The University of Arizona.