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Dictionary » Galloway syndrome

Galloway syndrome

Introduction: Galloway syndrome

Description of Galloway syndrome

Galloway syndrome (medical condition): A rare genetic disorder primarily involving physical and developmental...more »

See also:

Galloway syndrome:
  »Introduction: Galloway syndrome
  »Symptoms of Galloway syndrome

Galloway syndrome: Rare Disease

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

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


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

Source - Orphanet

Galloway syndrome as a Disease

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

Galloway syndrome: Related Diseases

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

More information on medical condition: Galloway syndrome:

Galloway syndrome: Related Disease Topics

These medical disease topics may be related to Galloway syndrome:

Terms associated with Galloway syndrome:

Terms Similar to Galloway syndrome:

Source - NIH

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