Spondylometaphyseal Dysplasia, Corner Fracture Type (SMDCF)

Spondylometaphyseal Dysplasia, Corner Fracture Type, also known as spondylometaphyseal dysplasia, 'corner fracture' type, is related to spondyloepimetaphyseal dysplasia, strudwick type and coxa vara, and has symptoms including waddling gait An important gene associated with Spondylometaphyseal Dysplasia, Corner Fracture Type is FN1 (Fibronectin 1), and among its related pathways/superpathways are Cell adhesion_ECM remodeling and Integrins in angiogenesis. Affiliated tissues include bone and skin, and related phenotypes are abnormal vertebral morphology and short stature