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NYS2

Introduction: NYS2

Description of NYS2

NYS2 (medical condition): A dominantly inherited eye disorder characterized by...more »

See also:

Nystagmus 2, congenital, autosomal dominant:
  »Introduction: Nystagmus 2, congenital, autosomal dominant
  »Symptoms of Nystagmus 2, congenital, autosomal dominant

NYS2: Rare Disease

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

NYS2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that NYS2, or a subtype of NYS2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

NYS2 as a Disease

NYS2: Another name for Nystagmus 2, congenital, autosomal dominant (or close medical condition association).
  »Introduction: Nystagmus 2, congenital, autosomal dominant
  »Symptoms of Nystagmus 2, congenital, autosomal dominant

NYS2: Related Diseases

NYS2: NYS2 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of NYS2 (Nystagmus 2, congenital, autosomal dominant)

Some of the symptoms of NYS2 incude:

Terms associated with NYS2:

Terms Similar to NYS2:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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