osteogenesis imperfecta type 10

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Disease Overview

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the SERPINH1 gene.

Synonyms

OI type 10
OI type X
OI, type 10
OI10
SERPINH1 osteogenesis imperfecta
osteogenesis imperfecta caused by mutation in SERPINH1
osteogenesis imperfecta type X
osteogenesis imperfecta, type 10
osteogenesis imperfecta, type X

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.