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WM syndrome (medical condition): A rare genetic disorder characterized by short stature, and craniofacial, eye,...more »
WM syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that WM syndrome, or a subtype of WM syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
WM syndrome: Another name for Spherophakia brachymorphia syndrome (or close medical condition association).
»Introduction: Spherophakia brachymorphia syndrome
»Symptoms of Spherophakia brachymorphia syndrome
WM syndrome: WM syndrome is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of WM syndrome incude:
These medical disease topics may be related to WM syndrome:
Source - NIH
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