Cleft Palate, X-linked

Overview of Cleft Palate, X-linked

Most recent studies have shown that Cleft Palate, X-linked shares some biological mechanisms with atresia, cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, congenital-abnormality, craniofacial-abnormalities, developmental-absence-of-tooth, digeorge-syndrome, dysplasia, genetic-diseases-x-linked, hypodontia, mandibulofacial-dysostosis, pelizaeus-merzbacher-disease, pterygium, rosselli-gulienetti-syndrome, sex-chromosome-aberrations, steroid-sulfatase-deficiency-disease, submucous-cleft-of-hard-palate, tongue-diseases, tongue-tie.

Among the many pathways, these few ones have gauged particular interests from scientists studying Cleft Palate, X-linked, and have been seen in publications frequently: Amelogenesis, Cell Proliferation, Conjugation, Localization, Mating, Metaphase, Ossification, Palate Development, Pathogenesis, Tongue Development

Quite a number of genes have been found to play important roles in Cleft Palate, X-linked, such as BMP4, CCND2, CPA1, CPOX, EBP, ESX1, FGF8, IRF6, KLHL2, KLHL4, MSX1, MTSS1, PGK1, PRM1, RPLP1, STS, TBX22, TNIP1. 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.

Cleft Palate, X-linked Related Genes

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Pathways Related to Cleft Palate, X-linked

This information is being compiled and will come in a future update

Related Diseases