osteogenesis imperfecta type 8

Rare Disease

MONDO:0012581

Also known as:

OI8P3H1 osteogenesis imperfectaosteogenesis imperfecta caused by mutation in P3H1

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the P3H1 gene.

Genes

Clinical Trials

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Newborn Screening

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Patient Groups

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Companies Active in osteogenesis imperfecta type 8

2 companies

Organizations with orphan designations or approved therapies for this disease

Angitia Biopharmaceuticals Guangzhou Limited

Other

Designated

Merck, Sharpe & Dohme Corp.