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Schinzel syndrome

Introduction: Schinzel syndrome

Description of Schinzel syndrome

Schinzel syndrome (medical condition): A very rare inherited disorder that involves the arm bones and...more »

See also:

Schinzel Syndrome:
  »Introduction: Schinzel Syndrome
  »Symptoms of Schinzel Syndrome

Schinzel syndrome: Rare Disease

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

Schinzel syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Schinzel syndrome, or a subtype of Schinzel 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 Schinzel syndrome as a "rare disease".

Source - Orphanet

Schinzel syndrome as a Disease

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

Schinzel syndrome: Related Diseases

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

More information on medical condition: Schinzel Syndrome:

Schinzel syndrome: Related Disease Topics

These medical disease topics may be related to Schinzel syndrome:

  • hypolasia
  • apocrine glands
  • hypoplastic terminal phalanx
  • mammary gland dysfunction

Terms associated with Schinzel syndrome:

Terms Similar to Schinzel syndrome:

Source - NIH

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