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Disease Info Card
Multiple Epiphyseal Dysplasia
Information about Multiple Epiphyseal Dysplasia: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Multiple Epiphyseal Dysplasia
Most recent studies have shown that Multiple Epiphyseal Dysplasia shares some biological mechanisms with abnormal-degeneration, achondroplasia, arthropathy, atelosteogenesis, bone-diseases-developmental, chondrodysplasia-punctata, congenital-abnormality, degenerative-polyarthritis, diastrophic-dysplasia, dwarfism, dysplasia, legg-calve-perthes-disease, osteochondrodysplasias, pain, pseudoachondroplastic-spondyloepiphyseal-dysplasia-syndrome, skeletal-dysplasia, spondyloepiphyseal-dysplasia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Multiple Epiphyseal Dysplasia, and have been seen in publications frequently: Aging, Bone Development, Cartilage Development, Cell Cycle, Cell Death, Chondrocyte Differentiation, Chondrocyte Proliferation, Endochondral Ossification, Ossification, Pathogenesis, Protein Folding, Protein Secretion, Proteolysis, Secretion, Sulfate Transport, Sulfation, Tissue Development, Translation, Transport, Transposition
Quite a number of genes have been found to play important roles in Multiple Epiphyseal Dysplasia, such as ACAN, ATP8A2, COL2A1, COL9A1, COL9A2, COL9A3, COMP, EGF, EIF2AK3, MATN3, NQO1, SCN8A, SLC25A5, SLC26A2, THBS1, TNC, VWF. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.