Disease Info Card

Anhydrotic Ectodermal Dysplasias

Information about Anhydrotic Ectodermal Dysplasias: 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 Anhydrotic Ectodermal Dysplasias

Most recent studies have shown that Anhydrotic Ectodermal Dysplasias shares some biological mechanisms with anhidrosis, bloch-sulzberger-syndrome, cattle-diseases, christ-siemens-touraine-syndrome, congenital-abnormality, congenital-absence, dermatologic-disorders, developmental-absence-of-tooth, dysplasia, ectodermal-dysplasia, fever-of-unknown-origin, hereditary-diseases, hypodontia, hypohidrosis, hypoplasia, hypotrichosis, immunologic-deficiency-syndromes, infective-disorder, rhinitis-atrophic, tooth-abnormalities.

Among the many pathways, these few ones have gauged particular interests from scientists studying Anhydrotic Ectodermal Dysplasias, and have been seen in publications frequently: Aging, Amelogenesis, Appendage Development, Cell Activation, Cell Adhesion, Cell-matrix Adhesion, Cellular Senescence, Dentinogenesis, Hair Follicle Development, Hair Follicle Morphogenesis, Inflammatory Response, Keratinization, Localization, Pathogenesis, Regulation Of Signaling, Respiratory Burst, Secretion, T Cell Activation, Translation, Transport

Quite a number of genes have been found to play important roles in Anhydrotic Ectodermal Dysplasias, such as CHUK, EDA, EDAR, EDARADD, IKBKB, IKBKE, IKBKG, IRAK4, LEF1, NFKB1, NFKBIA, TNF, TP63. 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.