GTR Home > Conditions/Phenotypes > Osteogenesis imperfecta, type XI

Summary

Osteogenesis imperfecta (OI) comprises a group of connective tissue disorders characterized by bone fragility and low bone mass. The disorder is clinically and genetically heterogeneous. OI type XI is an autosomal recessive form of OI (summary by Alanay et al., 2010). [from OMIM]

Available tests

31 tests are in the database for this condition.

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Genes See tests for all associated and related genes

  • Also known as: BRKS1, FKBP65, OI11, OI6, PPIASE, hFKBP65, FKBP10
    Summary: FKBP prolyl isomerase 10

Clinical features

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