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Retinoschisis, autosomal dominant

Retinoschisis, autosomal dominant: Introduction

Retinoschisis, autosomal dominant: A dominantly inherited disease of the retina. More detailed information about the symptoms, causes, and treatments of Retinoschisis, autosomal dominant is available below.

Symptoms of Retinoschisis, autosomal dominant

Home Diagnostic Testing

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Retinoschisis, autosomal dominant: Complications

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Causes of Retinoschisis, autosomal dominant

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Retinoschisis, autosomal dominant: Undiagnosed Conditions

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Retinoschisis, autosomal dominant: Research Doctors & Specialists

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Retinoschisis, autosomal dominant: Animations

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Retinoschisis, autosomal dominant: Broader Related Topics

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Definitions of Retinoschisis, autosomal dominant:

Retinoschisis, autosomal dominant is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Retinoschisis, autosomal dominant, or a subtype of Retinoschisis, autosomal dominant, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Retinoschisis, autosomal dominant Info

More information about Retinoschisis, autosomal dominant

  1. Retinoschisis, autosomal dominant: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
 

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