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osteogenesis imperfecta type 16

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

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Disease Overview

An osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11.

Synonyms

  • OI, type 16
  • OI16
  • chromosome 11P11.2 deletion syndrome, 91.3-Kb
  • chromosome 11p11.2 deletion syndrome 91.3-KB
  • osteogenesis imperfecta type XVI
  • osteogenesis imperfecta, type 16
  • osteogenesis imperfecta, type XVI
GARD Disease Summary

The Genetic and Rare Diseases Information Center (GARD) has information and resources for patients, caregivers, and families that may be helpful before and after diagnosis of this condition. GARD is a program of the National Center for Advancing Translational Sciences (NCATS), part of the National Institutes of Health (NIH).

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OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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