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WS 2

Introduction: WS 2

Description of WS 2

WS 2 (medical condition): A hereditary, autosomal dominant disorder....more »

See also:

Waardenburg syndrome type 2:
  »Introduction: Waardenburg syndrome type 2
  »Symptoms of Waardenburg syndrome type 2

WS 2: Rare Disease

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

WS 2 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that WS 2, or a subtype of WS 2, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

WS 2 as a Disease

WS 2: Another name for Waardenburg syndrome type 2 (or close medical condition association).
  »Introduction: Waardenburg syndrome type 2
  »Symptoms of Waardenburg syndrome type 2

WS 2: Related Diseases

WS 2: WS 2 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of WS 2 (Waardenburg syndrome type 2)

Some of the symptoms of WS 2 incude:

WS 2: Related Disease Topics

These medical disease topics may be related to WS 2:

Terms associated with WS 2:

Terms Similar to WS 2:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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