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Disease Info Card
Bullous Congenital Ichthyosiform Erythroderma (disorder)
Information about Bullous Congenital Ichthyosiform Erythroderma (disorder): 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 Bullous Congenital Ichthyosiform Erythroderma (disorder)
Most recent studies have shown that Bullous Congenital Ichthyosiform Erythroderma (disorder) shares some biological mechanisms with bulla, congenital-nonbullous-ichthyosiform-erythroderma, dermatologic-disorders, epidermolysis-bullosa, exfoliative-dermatitis, hyperkeratosis, ichthyoses, ichthyosiform-erythroderma-congenital, ichthyosis-bullosa-of-siemens, keratoderma-palmoplantar-epidermolytic, keratosis, melanocytic-nevus, palmoplantar-keratosis, skin-diseases-genetic, skin-diseases-vesiculobullous, skin-neoplasms.
Among the many pathways, these few ones have gauged particular interests from scientists studying Bullous Congenital Ichthyosiform Erythroderma (disorder), and have been seen in publications frequently: Cell Adhesion, Cell Differentiation, Cell Growth, Cell Proliferation, Cornification, Cytokinesis, Cytolysis, Hyperphosphorylation, Hypersensitivity, Immune Response, Keratinization, Keratinocyte Differentiation, Lipid Storage, Localization, Mitosis, Pathogenesis, Pigmentation, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Bullous Congenital Ichthyosiform Erythroderma (disorder), such as FLG, GDI1, GJB2, GJB3, GJB4, IVL, KRT1, KRT10, KRT14, KRT16, KRT2, KRT5, TGM1. 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.