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Disease Info Card
Campomelic Dysplasia
Information about Campomelic 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 Campomelic Dysplasia
Most recent studies have shown that Campomelic Dysplasia shares some biological mechanisms with bone-diseases-developmental, chromosomal-translocation, cleft-palate, congenital-abnormality, congenital-anomaly-of-skeletal-bone, congenital-clubfoot, cytogenetic-abnormality, disorders-of-sex-development, dwarfism, dysplasia, gonadal-dysgenesis, haploinsufficiency, hypoplasia, osteochondrodysplasias, osteogenesis-imperfecta, pierre-robin-syndrome, respiratory-distress, skeletal-dysplasia, thanatophoric-dysplasia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Campomelic Dysplasia, and have been seen in publications frequently: Brain Development, Cell Differentiation, Cell Fate Determination, Chondrocyte Differentiation, Fertilization, Gastrulation, Gene Conversion, Gonad Development, Interphase, Leydig Cell Differentiation, Lung Development, Male Sex Determination, Muscle Cell Differentiation, Ossification, Osteoblast Differentiation, Pathogenesis, Regulation Of Gene Expression, Sertoli Cell Differentiation, Sex Determination, Sex Differentiation
Quite a number of genes have been found to play important roles in Campomelic Dysplasia, such as ACD, CDKN2B, CHERP, COL11A2, COL2A1, CYFIP1, KDM5D, NR0B1, NR5A1, SF1, SOX10, SOX5, SOX8, SOX9, SRA1, SRY, SS18L1. 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.