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Disease Info Card
Otopalatodigital Syndrome, Type Ii
Information about Otopalatodigital Syndrome, Type Ii: 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 Otopalatodigital Syndrome, Type Ii
Most recent studies have shown that Otopalatodigital Syndrome, Type Ii shares some biological mechanisms with atelosteogenesis, bone-diseases-developmental, cleft-palate, complete-hearing-loss, conductive-hearing-loss, congenital-abnormality, congenital-exomphalos, congenital-omphalocele, craniofacial-abnormalities, dysplasia, ectopic-tissue, genetic-diseases-x-linked, hypoplasia, limb-deformities-congenital, melnick-needles-syndrome, osteochondrodysplasias, periventricular-nodular-heterotopia, skeletal-dysplasia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Otopalatodigital Syndrome, Type Ii, and have been seen in publications frequently: Bone Remodeling, Cell Motility, Dna Amplification, Endochondral Ossification, Intramembranous Ossification, Localization, Ossification
Quite a number of genes have been found to play important roles in Otopalatodigital Syndrome, Type Ii, such as AOX1, DMD, FLNA, FLNB, FLNC, GYPA, GYPE, PITX2, UTRN. 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 Otopalatodigital Syndrome, Type Ii
This information is being compiled and will come in a future update
| Bone Remodeling | Cell Motility | Dna Amplification |
| Endochondral Ossification | Intramembranous Ossification | Localization |
| Ossification |