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Disease Info Card
Mandibulofacial Dysostosis
Information about Mandibulofacial Dysostosis: 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 Mandibulofacial Dysostosis
Most recent studies have shown that Mandibulofacial Dysostosis shares some biological mechanisms with cleft-lip, cleft-palate, complete-hearing-loss, conductive-hearing-loss, congenital-abnormality, craniofacial-abnormalities, craniofacial-dysostosis, dermoid-cyst, dysostoses, dysplasia, eye-abnormalities, eye-neoplasms, facial-asymmetry, fetal-growth-retardation, goldenhar-syndrome-with-ipsilateral-radial-defect, hallermanns-syndrome, hypoplasia, micrognathism, pierre-robin-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mandibulofacial Dysostosis, and have been seen in publications frequently: Cell Cycle, Cell Death, Cell Migration, Ear Development, Fertilization, Head Segmentation, Interphase, Limb Development, Localization, Neural Crest Cell Development, Neural Crest Cell Migration, Ossification, Pathogenesis, Programmed Cell Death, Reflex, Regeneration, Ribosome Biogenesis, Segmentation, Translation, Transposition
Quite a number of genes have been found to play important roles in Mandibulofacial Dysostosis, such as CD55, CYLD, DHODH, EFTUD2, FGF1, HES1, HMMR, HNRNPC, NOLC1, PAFAH1B1, PITX1, POLR1C, POLR1D, PRRX1, SPARC, SS18L1, TCN2, TCOF1, TP53. 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.