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Dictionary » ORW disease
 

ORW disease

Introduction: ORW disease

Description of ORW disease

ORW disease (medical condition): A rare genetic disorder characterized by epistaxes and multiple...more »

See also:

Hereditary hemorrhagic telangiectasia:
  »Introduction: Hereditary hemorrhagic telangiectasia
  »Symptoms of Hereditary hemorrhagic telangiectasia

ORW disease: Rare Disease

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

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

ORW disease as a Disease

ORW disease: Another name for Hereditary hemorrhagic telangiectasia (or close medical condition association).
  »Introduction: Hereditary hemorrhagic telangiectasia
  »Symptoms of Hereditary hemorrhagic telangiectasia

ORW disease: Related Diseases

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

Symptoms of ORW disease (Hereditary hemorrhagic telangiectasia)

Some of the symptoms of ORW disease incude:

  • Pinpoint telangiectases
  • Spider telangiectases
  • Nodular telangiectases
  • Tongue telangiectases
  • Lip mucosa telangiectases

ORW disease: Related Disease Topics

These medical disease topics may be related to ORW disease:

  • autoosmal dominnat disorder
  • vascular abnormalities
  • recurrent spontaneous epistaxis
  • multiple telangiectasia
  • heart failure

Terms associated with ORW disease:

Terms Similar to ORW disease:

Source - NIH

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