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- Table of Contents
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Disease Info Card
Clinodactyly
Information about Clinodactyly: 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 Clinodactyly
Most recent studies have shown that Clinodactyly shares some biological mechanisms with brachydactyly, congenital-abnormality, congenital-hand-deformities, congenital-heart-defects, cytogenetic-abnormality, developmental-delay-(disorder), dwarfism, dysplasia, growth-disorders, growth-retardation, hypoplasia, low-set-ears, microcephaly, micrognathism, muscle-hypotonia, orbital-separation-excessive, syndactyly, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Clinodactyly, and have been seen in publications frequently: Bone Maturation, Cardiac Conduction, Developmental Process, Dna Methylation, Dosage Compensation, Embryonic Limb Morphogenesis, Fertilization, Hypersensitivity, Interphase, Limb Development, Meiosis, Meiosis I, Meiosis Ii, Menarche, Metaphase, Methylation, Neurogenesis, Ossification, Pathogenesis, Pigmentation
Quite a number of genes have been found to play important roles in Clinodactyly, such as AFP, CDK5R1, CDKN2B, CHP1, ENDOU, EXOSC6, IGF1R, INVS, KCNJ2, LMLN, NXT1, PES1, PTER, S100A10, SUB1, TMED9, TPPP, TWIST1. 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.