WS1 (medical condition): A hereditary, autosomal dominant disorder.
See also:
Waardenburg type 1:
»Introduction: Waardenburg type 1
»Symptoms of Waardenburg type 1
WS1 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that WS1, or a subtype of WS1,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
WS1: Another name for Waardenburg type 1 (or close medical condition association).
»Introduction: Waardenburg type 1
»Symptoms of Waardenburg type 1
Some of the symptoms of WS1 incude:
See full list of 7 symptoms of WS1 (Waardenburg type 1)
Source - NIH
Search to find out more about WS1:
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