Osteofibrous Dysplasia (OSFD)

Alias:
Ofd
Osfd
Tibia, Bowing of, with Pseudarthrosis and Pectus Excavatum
Bowing of Tibia with Pseudarthrosis and Pectus Excavatum
Dysplasia, Osteofibrous, Susceptibility to
Osteofibrous Dysplasia, Susceptibility to
Jaffe-Campanacci Syndrome
Ossifying Fibroma
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Osteofibrous Dysplasia, also known as ofd, is related to fibrous dysplasia and osteoblastoma. An important gene associated with Osteofibrous Dysplasia is MET (MET Proto-Oncogene, Receptor Tyrosine Kinase), and among its related pathways/superpathways are Signaling by Receptor Tyrosine Kinases and Binding and Uptake of Ligands by Scavenger Receptors. Affiliated tissues include bone and cortex, and related phenotypes are pectus excavatum and fibular hypoplasia
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
Unknown
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6
95
9

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
Related Gene
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Publications
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References Literature

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