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Disease Info Card
Acrodysostosis
Information about Acrodysostosis: 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 Acrodysostosis
Most recent studies have shown that Acrodysostosis shares some biological mechanisms with bone-diseases, bone-diseases-developmental, brachydactyly, congenital-abnormality, congenital-foot-deformity, congenital-hand-deformities, craniofacial-dysostosis, cytogenetic-abnormality, dwarfism, dysostoses, dysplasia, epiphysis-disorders, growth-disorders, hypoplasia, nose-deformities-acquired, osteochondrodysplasias, pseudohypoparathyroidism, pseudopseudohypoparathyroidism, skeletal-dysplasia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Acrodysostosis, and have been seen in publications frequently: Bone Maturation, Methylation, Ossification, Pathogenesis, Pigmentation, Protein Phosphorylation
Quite a number of genes have been found to play important roles in Acrodysostosis, such as APC, ENO1, FZD4, GNAS, GPR151, INS, LGR6, LPAR3, MRGPRX1, MRGPRX3, MRGPRX4, OXER1, PAH, PDE4D, PRKAR1A, PTH, PTRH1, WDTC1. 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.
Pathways Related to Acrodysostosis
This information is being compiled and will come in a future update
| Bone Maturation | Methylation | Ossification |
| Pathogenesis | Pigmentation | Protein Phosphorylation |