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Dictionary » LQT7
 

LQT7

Introduction: LQT7

Description of LQT7

LQT7 (medical condition): A rare disorder where a genetic mutation causes periods of muscle weakness,...more »

See also:

Andersen-Tawil syndrome:
  »Introduction: Andersen-Tawil syndrome
  »Symptoms of Andersen-Tawil syndrome

LQT7: Rare Disease

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

LQT7 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that LQT7, or a subtype of LQT7, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

LQT7 as a Disease

LQT7: Another name for Andersen-Tawil syndrome (or close medical condition association).
  »Introduction: Andersen-Tawil syndrome
  »Symptoms of Andersen-Tawil syndrome

LQT7: Related Diseases

LQT7: LQT7 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of LQT7 (Andersen-Tawil syndrome)

Some of the symptoms of LQT7 incude:

LQT7: Related Disease Topics

These medical disease topics may be related to LQT7:

Terms associated with LQT7:

Terms Similar to LQT7:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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