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Osteogenesis imperfecta congenita, microcephaly, and cataracts (medical condition): A rare genetic connective tissue disorder charactedrized by blue sclerae,...more »
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Osteogenesis imperfecta congenita, microcephaly, and cataracts:
»Introduction: Osteogenesis imperfecta congenita, microcephaly, and cataracts
»Symptoms of Osteogenesis imperfecta congenita, microcephaly, and cataracts
These medical condition or symptom topics may be relevant to medical information for Osteogenesis imperfecta congenita, microcephaly, and cataracts:
Osteogenesis imperfecta congenita, microcephaly, and cataracts 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 congenita, microcephaly, and cataracts, or a subtype of Osteogenesis imperfecta congenita, microcephaly, and cataracts,
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 Osteogenesis imperfecta congenita, microcephaly, and cataracts as a "rare disease".
Source - Orphanet
Osteogenesis imperfecta congenita, microcephaly, and cataracts (medical condition): See Osteogenesis imperfecta congenita, microcephaly, and cataracts (disease information).
»Introduction: Osteogenesis imperfecta congenita, microcephaly, and cataracts
»Symptoms of Osteogenesis imperfecta congenita, microcephaly, and cataracts
Osteogenesis imperfecta congenita, microcephaly, and cataracts: Osteogenesis imperfecta congenita, microcephaly, and cataracts is listed as a type of (or associated with) the following medical conditions in our database:
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