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Dictionary » Autosomal dominant retinoschisis
 

Autosomal dominant retinoschisis

Introduction: Autosomal dominant retinoschisis

Description of Autosomal dominant retinoschisis

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

See also:

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

Autosomal dominant retinoschisis: Related Topics

These medical condition or symptom topics may be relevant to medical information for Autosomal dominant retinoschisis:

Autosomal dominant retinoschisis: Rare Disease

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

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

Autosomal dominant retinoschisis as a Disease

Autosomal dominant retinoschisis: Another name for Retinoschisis, autosomal dominant (or close medical condition association).
  »Introduction: Retinoschisis, autosomal dominant
  »Symptoms of Retinoschisis, autosomal dominant

Autosomal dominant retinoschisis: Related Diseases

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

Symptoms of Autosomal dominant retinoschisis (Retinoschisis, autosomal dominant)

Some of the symptoms of Autosomal dominant retinoschisis incude:

Terms associated with Autosomal dominant retinoschisis:

Terms Similar to Autosomal dominant retinoschisis:

Source - NIH

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