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Dictionary » Congenital warfarin syndrome
 

Congenital warfarin syndrome

Introduction: Congenital warfarin syndrome

Description of Congenital warfarin syndrome

Congenital warfarin syndrome (medical condition): Various physical and other abnormalities that can result from the use...more »

See also:

Warfarin syndrome:
  »Introduction: Warfarin syndrome
  »Symptoms of Warfarin syndrome

Congenital warfarin syndrome: Related Topics

These medical condition or symptom topics may be relevant to medical information for Congenital warfarin syndrome:

Congenital warfarin syndrome: Rare Disease

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

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

Congenital warfarin syndrome as a Disease

Congenital warfarin syndrome: Another name for Warfarin syndrome (or close medical condition association).
  »Introduction: Warfarin syndrome
  »Symptoms of Warfarin syndrome

Congenital warfarin syndrome: Related Diseases

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

Symptoms of Congenital warfarin syndrome (Warfarin syndrome)

Some of the symptoms of Congenital warfarin syndrome incude:

Congenital warfarin syndrome: Related Disease Topics

These medical disease topics may be related to Congenital warfarin syndrome:

Terms associated with Congenital warfarin syndrome:

Terms Similar to Congenital warfarin syndrome:

Source - NIH

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