WS 2 (medical condition): A hereditary, autosomal dominant disorder.
See also:
Waardenburg syndrome type 2:
»Introduction: Waardenburg syndrome type 2
»Symptoms of Waardenburg syndrome type 2
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: Another name for Waardenburg syndrome type 2 (or close medical condition association).
»Introduction: Waardenburg syndrome type 2
»Symptoms of Waardenburg syndrome type 2
Some of the symptoms of WS 2 incude:
See full list of 21 symptoms of WS 2 (Waardenburg syndrome type 2)
These medical disease topics may be related to WS 2:
Source - NIH
Search to find out more about WS 2:
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