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FGS

Introduction: FGS

Description of FGS

FGS (medical condition): A rare genetic disorder characterized by anal...more »

See also:

FG Syndrome:
  »Introduction: FG Syndrome
  »Symptoms of FG Syndrome

FGS: Rare Disease

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

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

FGS as a Disease

FGS: Another name for FG Syndrome (or close medical condition association).
  »Introduction: FG Syndrome
  »Symptoms of FG Syndrome

FGS: Related Diseases

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

Symptoms of FGS (FG Syndrome)

Some of the symptoms of FGS incude:

FGS: Related Disease Topics

These medical disease topics may be related to FGS:

Terms associated with FGS:

Terms Similar to FGS:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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