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Disease Info Card
Short Rib-polydactyly Syndrome
Information about Short Rib-polydactyly 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 Short Rib-polydactyly Syndrome
Most recent studies have shown that Short Rib-polydactyly Syndrome shares some biological mechanisms with bone-diseases-developmental, cleft-lip, congenital-abnormality, dwarfism, dysplasia, edema, ellis-van-creveld-syndrome, fetal-death, fetal-diseases, hypoplasia, jeune-thoracic-dystrophy, micromelia, orofaciodigital-syndromes, osteochondrodysplasias, polydactyly, short-rib-polydactyly-syndrome-majewski-type, skeletal-dysplasia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Short Rib-polydactyly Syndrome, and have been seen in publications frequently: Cell Division, Dentinogenesis, Endochondral Ossification, Intraflagellar Transport, Ossification, Pathogenesis, Pigmentation, Segmentation, Transport
Quite a number of genes have been found to play important roles in Short Rib-polydactyly Syndrome, such as DYNC2H1, EVC, EVC2, FOXM1, IFT80, IGF1, IGF2, MTSS1, NEK1, OPN1LW, PCNT, RAB11FIP1, RFC1, RFC2, RICTOR, TCN2, UCN2, WDR19, WDR35. 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 Short Rib-polydactyly Syndrome
This information is being compiled and will come in a future update
| Cell Division | Dentinogenesis | Endochondral Ossification |
| Intraflagellar Transport | Ossification | Pathogenesis |
| Pigmentation | Segmentation | Transport |