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Dictionary » WS2B


Introduction: WS2B

Description of WS2B

WS2B (medical condition): A hereditary, autosomal dominant disorder....more »

See also:

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

WS2B: Rare Disease

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

WS2B is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that WS2B, or a subtype of WS2B, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

WS2B as a Disease

WS2B: Another name for Waardenburg syndrome type 2B (or close medical condition association).
  »Introduction: Waardenburg syndrome type 2B
  »Symptoms of Waardenburg syndrome type 2B

WS2B: Related Diseases

WS2B: WS2B is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of WS2B (Waardenburg syndrome type 2B)

Some of the symptoms of WS2B incude:

WS2B: Related Disease Topics

These medical disease topics may be related to WS2B:

  • rare genetic disorder
  • varying degrees of deafness
  • minor defects in structures arising from the neural crest
  • pigmentation anomalies

Terms associated with WS2B:

Terms Similar to WS2B:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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