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Dictionary » Retinoschisis autosomal dominant
 

Retinoschisis autosomal dominant

Introduction: Retinoschisis autosomal dominant

Description of Retinoschisis autosomal dominant

Retinoschisis autosomal dominant (medical condition): A dominantly inherited disease of the retina....more »

See also:

Retinoschisis, autosomal dominant:
  »Introduction: Retinoschisis, autosomal dominant
  »Symptoms of Retinoschisis, autosomal dominant

Retinoschisis autosomal dominant: Related Topics

These medical condition or symptom topics may be relevant to medical information for Retinoschisis autosomal dominant:

Retinoschisis autosomal dominant: Rare Disease

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

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)

Retinoschisis autosomal dominant as a Disease

Retinoschisis autosomal dominant (medical condition): See Retinoschisis, autosomal dominant (disease information).
  »Introduction: Retinoschisis, autosomal dominant
  »Symptoms of Retinoschisis, autosomal dominant

Retinoschisis autosomal dominant: Related Diseases

Retinoschisis autosomal dominant: Retinoschisis autosomal dominant is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Retinoschisis, autosomal dominant:

Terms associated with Retinoschisis autosomal dominant:

Terms Similar to Retinoschisis autosomal dominant:

Source - NIH

External links related to: Retinoschisis autosomal dominant

Source: Diseases Database

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