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Dictionary » Osteogenesis imperfecta type I
 

Osteogenesis imperfecta type I

Introduction: Osteogenesis imperfecta type I

Description of Osteogenesis imperfecta type I

Osteogenesis imperfecta type I (medical condition): A rare genetic connective tissue disorder characterized by...more »

See also:

Osteogenesis imperfecta Type I:
  »Introduction: Osteogenesis imperfecta Type I
  »Symptoms of Osteogenesis imperfecta Type I

Osteogenesis imperfecta type I: Related Topics

These medical condition or symptom topics may be relevant to medical information for Osteogenesis imperfecta type I:

Osteogenesis imperfecta type I: Rare Disease

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

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

Osteogenesis imperfecta type I as a Disease

Osteogenesis imperfecta type I (medical condition): See Osteogenesis imperfecta Type I (disease information).
  »Introduction: Osteogenesis imperfecta Type I
  »Symptoms of Osteogenesis imperfecta Type I

Osteogenesis imperfecta type I: Related Diseases

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

More information on medical condition: Osteogenesis imperfecta Type I:

Osteogenesis imperfecta type I: Related Disease Topics

These medical disease topics may be related to Osteogenesis imperfecta type I:

Terms associated with Osteogenesis imperfecta type I:

Terms Similar to Osteogenesis imperfecta type I:

Source - NIH

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Medical dictionaries:

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