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Disease Info Card
Hay-wells Syndrome Of Ectodermal Dysplasia
Information about Hay-wells Syndrome Of 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 Hay-wells Syndrome Of Ectodermal Dysplasia
Most recent studies have shown that Hay-wells Syndrome Of Ectodermal Dysplasia shares some biological mechanisms with adult-syndrome, ankyloblepharon-filiforme-adnatum, cleft-lip, cleft-palate, cleft-palate-with-cleft-lip, congenital-abnormality, dermatitis, dysplasia, ectodermal-dysplasia, ectrodactyly, ectrodactyly-ectodermal-dysplasia-clefting-syndrome, eye-abnormalities, hereditary-diseases, hypoplasia, limb-deformities-congenital, nails-malformed, rapp-hodgkin-syndrome, scalp-dermatoses, tissue-adhesions.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hay-wells Syndrome Of Ectodermal Dysplasia, and have been seen in publications frequently: Cell Growth, Cell Proliferation, Cell-cell Adhesion, Cytolysis, Defecation, Dna Repair, Gland Development, Keratinocyte Proliferation, Limb Development, Pathogenesis, Pigmentation, Sweat Gland Development, Wound Healing
Quite a number of genes have been found to play important roles in Hay-wells Syndrome Of Ectodermal Dysplasia, such as ARHGAP24, CDKN1A, CDKN1C, CKAP4, FGFR2, HNRNPAB, ITCH, MTSS1, PAK3, RPE65, SAMHD1, SFN, SMG1, TP53, TP63, TP73, 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.