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Disease Info Card
Ichthyosis, X-linked
Information about Ichthyosis, X-linked: 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 Ichthyosis, X-linked
Most recent studies have shown that Ichthyosis, X-linked shares some biological mechanisms with bullous-congenital-ichthyosiform-erythroderma-(disorder), chondrodysplasia-punctata, congenital-ichthyosis, congenital-nonbullous-ichthyosiform-erythroderma, cryptorchidism, deficiency-of-sulfatase, dermatologic-disorders, exfoliative-dermatitis, hyperkeratosis, hypogonadism, ichthyoses, ichthyosiform-erythroderma-congenital, ichthyosis-vulgaris, kallmann-syndrome, keratosis, sex-chromosome-aberrations, steroid-sulfatase-deficiency-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Ichthyosis, X-linked, and have been seen in publications frequently: Brain Development, Cell Cycle, Cell Maturation, Cell Proliferation, Cornification, Dosage Compensation, Excretion, Hair Follicle Morphogenesis, Immune Response, Interphase, Keratinization, Lipid Storage, Localization, Male Meiosis, Meiosis, Metaphase, Pathogenesis, Pigmentation, Secretion, Transport
Quite a number of genes have been found to play important roles in Ichthyosis, X-linked, such as ARSA, ARSH, CHP1, CS, DCTN3, DYNC1H1, ERMAP, FGFR1, FLG, PHB2, PYCARD, STS, SULT2A1, TGM1, VCX, VCX3A, XG. 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.