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Dictionary » Osteogenesis imperfecta tarda
 

Osteogenesis imperfecta tarda

Introduction: Osteogenesis imperfecta tarda

Description of Osteogenesis imperfecta tarda

Osteogenesis imperfecta tarda (medical condition): A genetic condition characterized mainly by fragile...more »

See also:

OI, Type I:
  »Introduction: OI, Type I
  »Symptoms of OI, Type I
  »Causes of OI, Type I

Osteogenesis imperfecta tarda: Related Topics

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

Osteogenesis imperfecta tarda: Rare Disease

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

Osteogenesis imperfecta tarda 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 tarda, or a subtype of Osteogenesis imperfecta tarda, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Osteogenesis imperfecta tarda as a Disease

Osteogenesis imperfecta tarda: Another name for OI, Type I (or close medical condition association).
  »Introduction: OI, Type I
  »Symptoms of OI, Type I
  »Causes of OI, Type I

Osteogenesis imperfecta tarda: Related Diseases

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

Causes of Osteogenesis imperfecta tarda

Some of the causes of Osteogenesis imperfecta tarda are included in the list below:

  • The condition is inherited in an autosomal dominant manner

Symptoms of Osteogenesis imperfecta tarda (OI, Type I)

Some of the symptoms of Osteogenesis imperfecta tarda incude:

Terms associated with Osteogenesis imperfecta tarda:

Terms Similar to Osteogenesis imperfecta tarda:

Source - NIH

Interesting Medical Articles:

Medical dictionaries:

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