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Osteogenesis imperfecta tarda (medical condition): A genetic condition characterized mainly by fragile bones that fracture...more »
See also:
OI, Type I:
»Introduction: OI, Type I
»Symptoms of OI, Type I
»Causes of OI, Type I
These medical condition or symptom topics may be relevant to medical information for Osteogenesis imperfecta tarda:
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: 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: Osteogenesis imperfecta tarda is listed as a type of (or associated with) the following medical conditions in our database:
Some of the causes of Osteogenesis imperfecta tarda are included in the list below:
Read more about causes of Osteogenesis imperfecta tarda (OI, Type I)
Some of the symptoms of Osteogenesis imperfecta tarda incude:
See full list of 9 symptoms of Osteogenesis imperfecta tarda (OI, Type I)
Source - NIH
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