GTR Home > Conditions/Phenotypes > Osteogenesis imperfecta type 7


Osteogenesis imperfecta is a connective tissue disorder characterized by bone fragility and low bone mass. OI type VII is an autosomal recessive form of severe or lethal OI (summary by Barnes et al., 2006). [from OMIM]

Available tests

44 tests are in the database for this condition.

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Genes See tests for all associated and related genes

  • Also known as: CASP, LEPREL3, OI7, P3H5, CRTAP
    Summary: cartilage associated protein

Clinical features


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