Osteogenesis Imperfecta, Type Xiv (OI14)

Alias:

Osteogenesis Imperfecta Type 14

Oi14

Osteogenesis Imperfecta Type Xiv

Osteogenesis Imperfecta 14

Oi, Type Xiv

Oi Type Xiv

Oi-Xiv

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Osteogenesis Imperfecta, Type Xiv, also known as osteogenesis imperfecta type 14, is related to brittle bone disorder and king-denborough syndrome. An important gene associated with Osteogenesis Imperfecta, Type Xiv is TMEM38B (Transmembrane Protein 38B), and among its related pathways/superpathways are Collagen chain trimerization and Extracellular matrix organization. Affiliated tissues include bone and cortex, and related phenotypes are osteopenia and recurrent fractures

Related ID：

MALACARDS：OST109

OMIM：615066

MESH：D010013