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Disease Info Card
Oblique Facial Clefts
Information about Oblique Facial Clefts: 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 Oblique Facial Clefts
Most recent studies have shown that Oblique Facial Clefts shares some biological mechanisms with amniotic-band-syndrome, amniotic-bands, anophthalmos, cleft-face, cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, congenital-abnormality, congenital-anomaly-of-face, craniofacial-abnormalities, craniofacial-dysostosis, eye-abnormalities, facial-asymmetry, limb-deformities-congenital, microphthalmos, oligohydramnios, pregnancy-complications.
Among the many pathways, these few ones have gauged particular interests from scientists studying Oblique Facial Clefts, and have been seen in publications frequently: Bone Resorption, Cell Adhesion, Pathogenesis, Transposition
Quite a number of genes have been found to play important roles in Oblique Facial Clefts, such as BMP1, CALML3, COTL1, CP, CSRP3, FUT3, HPS4, SPECC1L, 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.
Pathways Related to Oblique Facial Clefts
This information is being compiled and will come in a future update
| Bone Resorption | Cell Adhesion | Pathogenesis |
| Transposition |