WS2A (medical condition): A hereditary, autosomal dominant disorder.
See also:
Waardenburg syndrome type 2A:
»Introduction: Waardenburg syndrome type 2A
»Symptoms of Waardenburg syndrome type 2A
WS2A is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that WS2A, or a subtype of WS2A,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
WS2A: Another name for Waardenburg syndrome type 2A (or close medical condition association).
»Introduction: Waardenburg syndrome type 2A
»Symptoms of Waardenburg syndrome type 2A
Some of the symptoms of WS2A incude:
See full list of 7 symptoms of WS2A (Waardenburg syndrome type 2A)
Source - NIH
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