WS2B (medical condition): A hereditary, autosomal dominant disorder.
See also:
Waardenburg syndrome type 2B:
»Introduction: Waardenburg syndrome type 2B
»Symptoms of Waardenburg syndrome type 2B
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: Another name for Waardenburg syndrome type 2B (or close medical condition association).
»Introduction: Waardenburg syndrome type 2B
»Symptoms of Waardenburg syndrome type 2B
Some of the symptoms of WS2B incude:
See full list of 7 symptoms of WS2B (Waardenburg syndrome type 2B)
Source - NIH
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