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Results 1 - 7 of 7 for Osteogenesis imperfecta type 16
  1. Osteogenesis imperfecta 
    ... Registry: Osteogenesis imperfecta type 15 Genetic Testing Registry: Osteogenesis imperfecta type 16 Genetic Testing Registry: Osteogenesis imperfecta type 17 Genetic ...
    https://medlineplus.gov/genetics/condition/osteogenesis-imperfecta - Genetics
  2. FKBP10 gene 
    ... C, Marini JC. Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to ... Epub 2012 Jul 16. Citation on PubMed or Free article on PubMed ...
    https://medlineplus.gov/genetics/gene/fkbp10 - Genetics
  3. Gnathodiaphyseal dysplasia 
    ... syndrome 2 Osteogenesis imperfecta with unusual skeletal lesions Osteogenesis imperfecta, Levin type Genetic Testing Registry: Gnathodiaphyseal dysplasia Gnathodiaphyseal dysplasia National ...
    https://medlineplus.gov/.../condition/gnathodiaphyseal-dysplasia - Genetics
  4. Respiratory Issues in OI (Osteogenesis Imperfecta Foundation) - PDF  
    Osteogenesis Imperfecta/Living With ... Osteogenesis Imperfecta ... Osteogenesis Imperfecta Foundation ... PDF
    https://oif.org/wp-content/uploads/2019/08/Respiratory_Issues.pdf - External Health Links
  5. Dentinogenesis imperfecta 
    ... also responsible for dentin dysplasia type II. Dentinogenesis imperfecta type I occurs as part of osteogenesis imperfecta, which is caused by mutations in one ...
    https://medlineplus.gov/genetics/condition/dentinogenesis-imperfecta - Genetics
  6. Osteogenesis imperfecta 
    Osteogenesis imperfecta (OI) is present at birth. It is often caused by a defect in the gene that produces type I collagen, an important building block of bone. There are many defects that can affect this ...
    https://medlineplus.gov/ency/article/001573.htm - Medical Encyclopedia
  7. Osteoporosis-pseudoglioma syndrome 
    ... carriers may have decreased bone mineral density. OPPG Osteogenesis imperfecta, ocular form Genetic Testing Registry: Osteoporosis with pseudoglioma ...
    https://medlineplus.gov/.../osteoporosis-pseudoglioma-syndrome - Genetics