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Disease Info Card
Oculo-dento-digital Syndrome
Information about Oculo-dento-digital Syndrome: 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 Oculo-dento-digital Syndrome
Most recent studies have shown that Oculo-dento-digital Syndrome shares some biological mechanisms with congenital-abnormality, congenital-hand-deformities, craniofacial-abnormalities, dental-enamel-hypoplasia, dysplasia, eye-abnormalities, glaucoma, hallermanns-syndrome, hypoplasia, limb-deformities-congenital, microphthalmos, odontodysplasia, paraparesis, paraparesis-spastic, syndactyly, syndactyly-of-fingers, tooth-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Oculo-dento-digital Syndrome, and have been seen in publications frequently: Aging, Bone Development, Bone Remodeling, Cell Differentiation, Gap Junction Assembly, Gastric Motility, Gland Development, Keratinocyte Differentiation, Lactation, Localization, Mammary Gland Development, Mating, Milk Ejection, Myelination, Osteoblast Differentiation, Parturition, Sertoli Cell Differentiation, Spermatogenesis, Tooth Eruption, Wound Healing
Quite a number of genes have been found to play important roles in Oculo-dento-digital Syndrome, such as BMP2, BMP4, EXOSC10, GJA1, GJA5, GJB1, GJB2, GJC1, GJC2, IVL, OSR1, PITX2, PMP2, RPLP2, SHH, TNFRSF11B. 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.