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Disease Info Card
Ichthyosiform Erythroderma, Congenital
Information about Ichthyosiform Erythroderma, Congenital: 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 Ichthyosiform Erythroderma, Congenital
Most recent studies have shown that Ichthyosiform Erythroderma, Congenital shares some biological mechanisms with bulla, bullous-congenital-ichthyosiform-erythroderma-(disorder), congenital-ichthyosis, congenital-nonbullous-ichthyosiform-erythroderma, dermatitis, dermatitis-atopic, dermatologic-disorders, exfoliative-dermatitis, hyperkeratosis, ichthyoses, ichthyosis-linearis-circumflexa, ichthyosis-vulgaris, ichthyosis-x-linked, melanocytic-nevus, psoriasis, skin-diseases-genetic, skin-diseases-vesiculobullous, skin-neoplasms, triglyceride-storage-disease-with-ichthyosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Ichthyosiform Erythroderma, Congenital, and have been seen in publications frequently: Brain Development, Cell Adhesion, Cell Proliferation, Cornification, Cytokinesis, Cytolysis, Diuresis, Exocytosis, Keratinization, Keratinocyte Differentiation, Keratinocyte Proliferation, Lipid Storage, Lipid Transport, Localization, Pathogenesis, Pigmentation, Proteolysis, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Ichthyosiform Erythroderma, Congenital, such as ABCA12, ABHD5, ALOX12, ALOX12B, ALOXE3, FLG, GJB2, KRT1, KRT10, KRT14, KRT16, KRT2, KRT5, PNPLA2, SPINK5, 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.