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LGS

Introduction: LGS

Description of LGS

LGS (medical condition): A rare genetic disorder characterized by bony growths,...more »

See also:

Trichorhinophalangeal syndrome type 2:
  »Introduction: Trichorhinophalangeal syndrome type 2
  »Symptoms of Trichorhinophalangeal syndrome type 2

LGS: Rare Disease

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

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

LGS as a Disease

LGS: Another name for Trichorhinophalangeal syndrome type 2 (or close medical condition association).
  »Introduction: Trichorhinophalangeal syndrome type 2
  »Symptoms of Trichorhinophalangeal syndrome type 2

LGS: Related Diseases

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

Symptoms of LGS (Trichorhinophalangeal syndrome type 2)

Some of the symptoms of LGS incude:

LGS: Related Disease Topics

These medical disease topics may be related to LGS:

Terms associated with LGS:

Terms Similar to LGS:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

More Medical Dictionary Topics

  • Weir Mitchell's disease
  • Weir-Mitchell disease
  • Weisbach
  • Weisbach angle
  • Weisenburg syndrome
  • Weismann
  • Weismann Netter Stuhl syndrome
  • Weismann Netter syndrome
  • Weismannism
  • Weiss
  • Weiss sign

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