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Iridogoniodysgenesis type1

Introduction: Iridogoniodysgenesis type1

Description of Iridogoniodysgenesis type1

Iridogoniodysgenesis type1 (medical condition): A rare genetic eye disorder involving glaucoma and iris anomalies and...more »

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Iridogoniodysgenesis type1:
  »Introduction: Iridogoniodysgenesis type1
  »Symptoms of Iridogoniodysgenesis type1

Iridogoniodysgenesis type1: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

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)

Iridogoniodysgenesis type1 as a Disease

Iridogoniodysgenesis type1 (medical condition): See Iridogoniodysgenesis type1 (disease information).
  »Introduction: Iridogoniodysgenesis type1
  »Symptoms of Iridogoniodysgenesis type1

Iridogoniodysgenesis type1: Related Diseases

Iridogoniodysgenesis type1: Iridogoniodysgenesis type1 is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Iridogoniodysgenesis type1:

Terms associated with Iridogoniodysgenesis type1:

Terms Similar to Iridogoniodysgenesis type1:

Source - NIH

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