Cleft Uvula

Overview of Cleft Uvula

Most recent studies have shown that Cleft Uvula shares some biological mechanisms with aneurysm, aortic-aneurysm, cleft-lip, cleft-palate, congenital-abnormality, craniofacial-abnormalities, developmental-delay-(disorder), diastasis, dysplasia, ear-inflammation, hypodontia, hypoplasia, loeys-dietz-syndrome, micrognathism, orbital-separation-excessive, otitis-media, pathological-dilatation, submucous-cleft-of-hard-palate, velopharyngeal-insufficiency.

Among the many pathways, these few ones have gauged particular interests from scientists studying Cleft Uvula, and have been seen in publications frequently: Bilateral Process, Fertilization, Gene Conversion, Limb Development, Localization, Mastication, Meiosis, Micturition, Nipple Development, Ossification, Pathogenesis, Sex Determination

Quite a number of genes have been found to play important roles in Cleft Uvula, such as BMP4, COL2A1, CP, CPOX, CYP21A2, ENG, IRF6, MB, POC1A, TBX1, TGFBR1, TGFBR2, TNIP1, TNXB, TP63, TWIST1. 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 Uvula Related Genes

click to see detail information for each gene

Pathways Related to Cleft Uvula

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

Related Diseases