Sillence syndrome

Introduction: Sillence syndrome

Description of Sillence syndrome

Sillence syndrome (medical condition): An extremely rare genetic disorder primarily involving digit abnormalities, scoliosis and club feet.

See also:

Sillence syndrome:
  »Introduction: Sillence syndrome
  »Symptoms of Sillence syndrome

Sillence syndrome: Rare Disease

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

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

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Sillence syndrome as a "rare disease".

Source - Orphanet

Sillence syndrome as a Disease

Sillence syndrome (medical condition): See Sillence syndrome (disease information).
  »Introduction: Sillence syndrome
  »Symptoms of Sillence syndrome

More information on medical condition: Sillence syndrome:

• Information about Sillence syndrome
• Basic Summary for Sillence syndrome
• Symptoms of Sillence syndrome

Terms associated with Sillence syndrome:

Terms Similar to Sillence syndrome:

• Brachydactyly-distal symphalangism syndrome

Source - NIH

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