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WS3

Introduction: WS3

Description of WS3

WS3 (medical condition): A rare syndrome involving deafness, pigmentation and musculoskeletal...more »

See also:

Waardenburg syndrome, type 3:
  »Introduction: Waardenburg syndrome, type 3
  »Symptoms of Waardenburg syndrome, type 3

WS3: Rare Disease

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

WS3 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that WS3, or a subtype of WS3, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

WS3 as a Disease

WS3: Another name for Waardenburg syndrome, type 3 (or close medical condition association).
  »Introduction: Waardenburg syndrome, type 3
  »Symptoms of Waardenburg syndrome, type 3

WS3: Related Diseases

WS3: WS3 is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of WS3 (Waardenburg syndrome, type 3)

Some of the symptoms of WS3 incude:

WS3: Related Disease Topics

These medical disease topics may be related to WS3:

  • rare genetic disorder
  • varying degrees of deafness
  • minor defects in structures arising from the neural crest
  • pigmentation anomalies

Terms associated with WS3:

Terms Similar to WS3:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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  • Syncytial knot
  • Syncytial sprout
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  • Syncytioma malignum

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