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Disease Info Card
Orofaciodigital Syndromes
Information about Orofaciodigital Syndromes: 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 Orofaciodigital Syndromes
Most recent studies have shown that Orofaciodigital Syndromes shares some biological mechanisms with cleft-lip, cleft-palate, congenital-abnormality, congenital-absence, congenital-hand-deformities, cystic-kidney-diseases, cytogenetic-abnormality, dysplasia, hamartoma, hydrocephalus, hypoplasia, kidney-diseases, mohr-syndrome, orbital-separation-excessive, orofaciodigital-syndrome-i, polycystic-kidney-diseases, polydactyly, syndactyly, tooth-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Orofaciodigital Syndromes, and have been seen in publications frequently: Beak Development, Bone Development, Cell Cycle, Cell Migration, Cell Proliferation, Chromosome Segregation, Cilium Assembly, Gastric Motility, Gastrulation, Interphase, Intraflagellar Transport, Limb Development, Limb Morphogenesis, Localization, Microtubule Depolymerization, Palate Development, Pathogenesis, Protein Import, Secretory Pathway, Transport
Quite a number of genes have been found to play important roles in Orofaciodigital Syndromes, such as AVP, CENPJ, CP, CPOX, GLI3, IFT88, KIF3A, MFN2, OFD1, PAFAH1B1, PCM1, SHH, SUCLG2, TCOF1, TIMM13, TIMM8A. 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.