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Disease Info Card
Ectodermal Dysplasia
Information about Ectodermal Dysplasia: 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 Ectodermal Dysplasia
Most recent studies have shown that Ectodermal Dysplasia shares some biological mechanisms with anhydrotic-ectodermal-dysplasias, aplasia-cutis-congenita, aplasia-nos, christ-siemens-touraine-syndrome, cleft-lip, cleft-palate, congenital-abnormality, dermatologic-disorders, developmental-absence-of-tooth, dysplasia, ectrodactyly, ectrodactyly-ectodermal-dysplasia-clefting-syndrome, hereditary-diseases, hypodontia, hypohidrosis, hypoplasia, hypotrichosis, nails-malformed, tooth-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Ectodermal Dysplasia, and have been seen in publications frequently: Amelogenesis, Appendage Development, Cell Adhesion, Cell Death, Cell Proliferation, Dentinogenesis, Dna Repair, Gland Development, Hair Follicle Development, Immune Response, Limb Development, Localization, Odontogenesis, Ossification, Pathogenesis, Pigmentation, Regeneration, Secretion, Skin Development, Translation
Quite a number of genes have been found to play important roles in Ectodermal Dysplasia, such as CKAP4, EDA, EDA2R, EDAR, EDARADD, GJB2, GJB6, HAND2, IKBKG, KRT16, KRT17, MAP2K1, NFKB1, RPE65, TNF, TP63, UVRAG. 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.