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Dictionary » Schwartz Jampel syndrome
 

Schwartz Jampel syndrome

Introduction: Schwartz Jampel syndrome

Description of Schwartz Jampel syndrome

Schwartz Jampel syndrome (medical condition): A rare genetic disorder characterized by myotonia, blepharophimosis and joint...more »

See also:

Schwartz-Jampel Syndrome:
  »Introduction: Schwartz-Jampel Syndrome
  »Symptoms of Schwartz-Jampel Syndrome

Schwartz Jampel syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for Schwartz Jampel syndrome:

Schwartz Jampel syndrome: Rare Disease

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

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

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Schwartz Jampel syndrome as a "rare disease".

Source - Orphanet

Schwartz Jampel syndrome as a Disease

Schwartz Jampel syndrome (medical condition): See Schwartz-Jampel Syndrome (disease information).
  »Introduction: Schwartz-Jampel Syndrome
  »Symptoms of Schwartz-Jampel Syndrome

Schwartz Jampel syndrome: Related Diseases

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

More information on medical condition: Schwartz-Jampel Syndrome:

Schwartz Jampel syndrome: Related Disease Topics

These medical disease topics may be related to Schwartz Jampel syndrome:

Terms associated with Schwartz Jampel syndrome:

Terms Similar to Schwartz Jampel syndrome:

Source - NIH

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