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Disease Info Card
Hidrotic Ectodermal Dysplasia
Information about Hidrotic 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 Hidrotic Ectodermal Dysplasia
Most recent studies have shown that Hidrotic Ectodermal Dysplasia shares some biological mechanisms with autosomal-dominant-hidrotic-ectodermal-dysplasia, christ-siemens-touraine-syndrome, dermatologic-disorders, developmental-absence-of-tooth, dysplasia, dystrophia-unguium, dystrophy, ectodermal-dysplasia, hyperkeratosis, hypodontia, hypotrichosis, keratosis, nail-diseases, nails-malformed, neoplasms, palmoplantar-keratosis, sweat-gland-neoplasms, tooth-abnormalities.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hidrotic Ectodermal Dysplasia, and have been seen in publications frequently: Catagen, Cornification, Interphase, Localization, Reverse Transcription
Quite a number of genes have been found to play important roles in Hidrotic Ectodermal Dysplasia, such as ACTA1, EVC, EVC2, FGF9, GJA1, GJB1, GJB2, GJB3, GJB4, GJB6, HAND2, RHCE, RHD, TUBA3C, TUBA3D. 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.
Pathways Related to Hidrotic Ectodermal Dysplasia
This information is being compiled and will come in a future update
| Catagen | Cornification | Interphase |
| Localization | Reverse Transcription |