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Disease Info Card
Congenital Musculoskeletal Anomalies
Information about Congenital Musculoskeletal Anomalies: 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 Congenital Musculoskeletal Anomalies
Most recent studies have shown that Congenital Musculoskeletal Anomalies shares some biological mechanisms with acquired-kyphosis, cardiovascular-abnormalities, congenital-abnormality, congenital-clubfoot, congenital-digestive-system-anomalies, congenital-funnel-chest, congenital-heart-defects, congenital-neurologic-anomalies, craniofacial-abnormalities, dwarfism, dysplasia, hypoplasia, musculoskeletal-diseases, myopathy, neoplasms, nervousness, pain, scoliosis-unspecified, urogenital-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Musculoskeletal Anomalies, and have been seen in publications frequently: Bone Development, Bone Mineralization, Bone Resorption, Cell Differentiation, Cell Migration, Cell Proliferation, Glycosylation, Innervation, Lactation, Limb Development, Locomotion, Muscle Atrophy, Ossification, Parturition, Pathogenesis, Pigmentation, Reflex, Segmentation, Swimming, Translation
Quite a number of genes have been found to play important roles in Congenital Musculoskeletal Anomalies, such as COL2A1, DMD, ELN, FBN1, FGFR3, GDF5, INS, KAT6B, MB, OCRL, PAX3, PES1, RYR1, SBDS, 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.