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Disease Info Card
Hypotelorism Of Orbit
Information about Hypotelorism Of Orbit: 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 Hypotelorism Of Orbit
Most recent studies have shown that Hypotelorism Of Orbit shares some biological mechanisms with alobar-holoprosencephaly, cebocephaly, cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, congenital-abnormality, craniofacial-abnormalities, craniosynostosis, cyclocephaly, cytogenetic-abnormality, developmental-delay-(disorder), dysplasia, eye-abnormalities, holoprosencephaly, hypoplasia, microcephaly, orbital-separation-excessive, trigonocephaly, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hypotelorism Of Orbit, and have been seen in publications frequently: Aging, Brain Development, Cell Death, Cell Division, Cell Killing, Cell Proliferation, Enucleation, Forebrain Development, Gastrulation, Hypersensitivity, Intraflagellar Transport, Localization, Mastication, Menopause, Ossification, Pathogenesis, Pigmentation, Segmentation, Translation, Transport
Quite a number of genes have been found to play important roles in Hypotelorism Of Orbit, such as BMP2, DLC1, FOXL2, HP, IL10, PMP22, PTCH1, RET, SHH, SIX3, SLC25A43, SS18L1, SSB, TGIF1, TWIST1, ZIC2. 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.