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LGMD3

Introduction: LGMD3

Description of LGMD3

LGMD3 (medical condition): An inherited muscle disease affecting mainly the upper...more »

See also:

Muscular Dystrophy, Limb-Girdle, Type 3:
  »Introduction: Muscular Dystrophy, Limb-Girdle, Type 3
  »Symptoms of Muscular Dystrophy, Limb-Girdle, Type 3
  »Causes of Muscular Dystrophy, Limb-Girdle, Type 3

LGMD3: Rare Disease

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

LGMD3 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that LGMD3, or a subtype of LGMD3, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

LGMD3 as a Disease

LGMD3: Another name for Muscular Dystrophy, Limb-Girdle, Type 3 (or close medical condition association).
  »Introduction: Muscular Dystrophy, Limb-Girdle, Type 3
  »Symptoms of Muscular Dystrophy, Limb-Girdle, Type 3
  »Causes of Muscular Dystrophy, Limb-Girdle, Type 3

LGMD3: Related Diseases

LGMD3: LGMD3 is listed as a type of (or associated with) the following medical conditions in our database:

Causes of LGMD3

Some of the causes of LGMD3 are included in the list below:

  • The condition is inherited in an autosomal recessive manner

Symptoms of LGMD3 (Muscular Dystrophy, Limb-Girdle, Type 3)

Some of the symptoms of LGMD3 incude:

Terms associated with LGMD3:

Terms Similar to LGMD3:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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