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WM syndrome

Introduction: WM syndrome

Description of WM syndrome

WM syndrome (medical condition): A rare genetic disorder characterized by short stature, and craniofacial, eye,...more »

See also:

Spherophakia brachymorphia syndrome:
  »Introduction: Spherophakia brachymorphia syndrome
  »Symptoms of Spherophakia brachymorphia syndrome

WM syndrome: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

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 as a Disease

WM syndrome: Another name for Spherophakia brachymorphia syndrome (or close medical condition association).
  »Introduction: Spherophakia brachymorphia syndrome
  »Symptoms of Spherophakia brachymorphia syndrome

WM syndrome: Related Diseases

WM syndrome: WM syndrome is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of WM syndrome (Spherophakia brachymorphia syndrome)

Some of the symptoms of WM syndrome incude:

WM syndrome: Related Disease Topics

These medical disease topics may be related to WM syndrome:

Terms associated with WM syndrome:

Terms Similar to WM syndrome:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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