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Iridogoniodysgenesis type1

Iridogoniodysgenesis type1: Introduction

Iridogoniodysgenesis type1: A rare genetic eye disorder involving glaucoma and iris anomalies and resulting in vision loss. More detailed information about the symptoms, causes, and treatments of Iridogoniodysgenesis type1 is available below.

Symptoms of Iridogoniodysgenesis type1

Home Diagnostic Testing

Home medical testing related to Iridogoniodysgenesis type1:

Wrongly Diagnosed with Iridogoniodysgenesis type1?

Causes of Iridogoniodysgenesis type1

Read more about causes of Iridogoniodysgenesis type1.

Iridogoniodysgenesis type1: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Iridogoniodysgenesis type1: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Iridogoniodysgenesis type1: Animations

Statistics for Iridogoniodysgenesis type1

Iridogoniodysgenesis type1: Broader Related Topics

User Interactive Forums

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Definitions of Iridogoniodysgenesis type1:

Iridogoniodysgenesis type1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Iridogoniodysgenesis type1, or a subtype of Iridogoniodysgenesis type1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Iridogoniodysgenesis type1 Info

More information about Iridogoniodysgenesis type1

  1. Iridogoniodysgenesis type1: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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