Ichthyosis Bullosa Of Siemens

Overview of Ichthyosis Bullosa Of Siemens

Most recent studies have shown that Ichthyosis Bullosa Of Siemens shares some biological mechanisms with bulla, bullous-congenital-ichthyosiform-erythroderma-(disorder), congenital-ichthyosis, dermatologic-disorders, epidermolysis-bullosa, exfoliative-dermatitis, hyperkeratosis, ichthyoses, ichthyosiform-erythroderma-congenital, leukokeratosis-hereditary-mucosal, melanocytic-nevus, monilethrix, pachyonychia-congenita, palmoplantar-keratosis, skin-diseases-genetic, skin-diseases-vesiculobullous, thickened-nails.

Among the many pathways, these few ones have gauged particular interests from scientists studying Ichthyosis Bullosa Of Siemens, and have been seen in publications frequently: Cell Cycle, Cell Proliferation, Cornification, Cytolysis, Keratinization, Pathogenesis, Pigmentation, Wound Healing

Quite a number of genes have been found to play important roles in Ichthyosis Bullosa Of Siemens, such as CTLA4, GDI1, KCNG1, KRT1, KRT10, KRT13, KRT14, KRT16, KRT17, KRT2, KRT4, KRT5, KRT86, MTSS1, NAT9. 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.

Ichthyosis Bullosa Of Siemens Related Genes

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Pathways Related to Ichthyosis Bullosa Of Siemens

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

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