Orofaciodigital Syndrome I

Overview of Orofaciodigital Syndrome I

Most recent studies have shown that Orofaciodigital Syndrome I shares some biological mechanisms with cleft-lip, cleft-palate, congenital-abnormality, congenital-absence, cystic-kidney-diseases, dysplasia, hamartoma, hydrocephalus, hypoplasia, kidney-diseases, mohr-syndrome, mouth-abnormalities, nervousness, orbital-separation-excessive, orofaciodigital-syndromes, polycystic-kidney-diseases, polydactyly, syndactyly, tooth-abnormalities.

Among the many pathways, these few ones have gauged particular interests from scientists studying Orofaciodigital Syndrome I, and have been seen in publications frequently: Cell Cycle, Chromosome Segregation, Interphase, Kidney Development, Localization, Mastication, Microtubule Depolymerization, Mitosis, Odontogenesis, Pathogenesis, Rna Interference, Tissue Homeostasis

Quite a number of genes have been found to play important roles in Orofaciodigital Syndrome I, such as ACACA, AHI1, CDKL1, CDKL5, CEP290, GLI3, GOLPH3, IKBKG, MBD1, MKS1, NPHP4, OFD1, PCM1, SDCCAG8, SHH, TMEM67, UMOD. 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.

Orofaciodigital Syndrome I Related Genes

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Pathways Related to Orofaciodigital Syndrome I

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

Related Diseases