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LGMD2

Introduction: LGMD2

Description of LGMD2

LGMD2 (medical condition): An autosomal recessive form of limb-girdle muscular dystrophy where...more »

See also:

Limb-Girdle muscular dystrophy type 2A:
  »Introduction: Limb-Girdle muscular dystrophy type 2A
  »Symptoms of Limb-Girdle muscular dystrophy type 2A

LGMD2: Rare Disease

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

LGMD2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that LGMD2, or a subtype of LGMD2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

LGMD2 as a Disease

LGMD2: Another name for Limb-Girdle muscular dystrophy type 2A (or close medical condition association).
  »Introduction: Limb-Girdle muscular dystrophy type 2A
  »Symptoms of Limb-Girdle muscular dystrophy type 2A

LGMD2: Related Diseases

LGMD2: LGMD2 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of LGMD2 (Limb-Girdle muscular dystrophy type 2A)

Some of the symptoms of LGMD2 incude:

LGMD2: Related Disease Topics

These medical disease topics may be related to LGMD2:

Terms associated with LGMD2:

Terms Similar to LGMD2:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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