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Dictionary » Familial foveal retinoschisis
 

Familial foveal retinoschisis

Introduction: Familial foveal retinoschisis

Description of Familial foveal retinoschisis

Familial foveal retinoschisis (medical condition): A rare genetic disorder where the retina splits resulting in slow,...more »

See also:

Retinoschisis of Fovea:
  »Introduction: Retinoschisis of Fovea
  »Symptoms of Retinoschisis of Fovea

Familial foveal retinoschisis: Related Topics

These medical condition or symptom topics may be relevant to medical information for Familial foveal retinoschisis:

Familial foveal retinoschisis: Rare Disease

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

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

Familial foveal retinoschisis as a Disease

Familial foveal retinoschisis: Another name for Retinoschisis of Fovea (or close medical condition association).
  »Introduction: Retinoschisis of Fovea
  »Symptoms of Retinoschisis of Fovea

Familial foveal retinoschisis: Related Diseases

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

Symptoms of Familial foveal retinoschisis (Retinoschisis of Fovea)

Some of the symptoms of Familial foveal retinoschisis incude:

  • Degeneration of the retina
  • Poor vision
  • Splitting of the retina

Familial foveal retinoschisis: Related Disease Topics

These medical disease topics may be related to Familial foveal retinoschisis:

Terms associated with Familial foveal retinoschisis:

Terms Similar to Familial foveal retinoschisis:

Source - NIH

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