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Dictionary » Leri-Weil syndrome
 

Leri-Weil syndrome

Introduction: Leri-Weil syndrome

Description of Leri-Weil syndrome

Leri-Weil syndrome (medical condition): A rare genetic disorder characterized by short forearms,...more »

See also:

Leri-Weil syndrome:
  »Introduction: Leri-Weil syndrome
  »Symptoms of Leri-Weil syndrome

Leri-Weil syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for Leri-Weil syndrome:

Leri-Weil syndrome: Rare Disease

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

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

Leri-Weil syndrome as a Disease

Leri-Weil syndrome (medical condition): See Leri-Weil syndrome (disease information).
  »Introduction: Leri-Weil syndrome
  »Symptoms of Leri-Weil syndrome

Leri-Weil syndrome: Related Diseases

Leri-Weil syndrome: Leri-Weil syndrome is listed as a type of (or associated with) the following medical conditions in our database:

More information on medical condition: Leri-Weil syndrome:

Leri-Weil syndrome: Related Disease Topics

These medical disease topics may be related to Leri-Weil syndrome:

Terms associated with Leri-Weil syndrome:

Terms Similar to Leri-Weil syndrome:

Source - NIH

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