Short Rib-polydactyly Syndrome, Majewski Type

Overview of Short Rib-polydactyly Syndrome, Majewski Type

Most recent studies have shown that Short Rib-polydactyly Syndrome, Majewski Type shares some biological mechanisms with cleft-lip, congenital-abnormality, dwarfism, dysplasia, ellis-van-creveld-syndrome, fetal-diseases, hypoplasia, jeune-thoracic-dystrophy, micromelia, mohr-syndrome, orofaciodigital-syndrome-i, orofaciodigital-syndromes, osteochondrodysplasias, osteogenesis-imperfecta, polydactyly, polysyndactyly, short-rib-polydactyly-syndrome, skeletal-dysplasia, thanatophoric-dysplasia.

Among the many pathways, these few ones have gauged particular interests from scientists studying Short Rib-polydactyly Syndrome, Majewski Type, and have been seen in publications frequently: Endochondral Ossification, Intraflagellar Transport, Ossification, Transport

Quite a number of genes have been found to play important roles in Short Rib-polydactyly Syndrome, Majewski Type, such as ATM, DYNC2H1, EVC, EVC2, IFT122, IFT43, IFT80, NEK1, RFXANK, TTC21B, 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.

Short Rib-polydactyly Syndrome, Majewski Type Related Genes

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Pathways Related to Short Rib-polydactyly Syndrome, Majewski Type

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

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