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Disease Info Card
Waardenburg Syndrome, Type 4a
Information about Waardenburg Syndrome, Type 4a: 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 Waardenburg Syndrome, Type 4a
Most recent studies have shown that Waardenburg Syndrome, Type 4a shares some biological mechanisms with complete-hearing-loss, congenital-abnormality, congenital-disorders, crest-syndrome, demyelinating-diseases, demyelinating-polyneuropathy, dysplasia, haploinsufficiency, hirschsprung-disease, hypopigmentation-disorder, intestinal-obstruction, leukodystrophy, megacolon, nervousness, sensorineural-hearing-loss-(disorder), total-colonic-aganglionosis, waardenburg-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Waardenburg Syndrome, Type 4a, and have been seen in publications frequently: Cell Development, Cell Migration, Cell Proliferation, Embryo Development, Enteric Nervous System Development, Innervation, Melanocyte Differentiation, Melanocyte Migration, Myelination, Nervous System Development, Neural Crest Cell Development, Neuron Development, Oligodendrocyte Differentiation, Pathogenesis, Pigment Cell Development, Pigmentation, Regeneration, System Development, Translation
Quite a number of genes have been found to play important roles in Waardenburg Syndrome, Type 4a, such as EDN3, EDNRB, ELN, GDNF, GJB1, GLB1, KITLG, MITF, MPZ, PAX3, RET, SOX10, SOX9, SRY, SS18L1, TYR, ZEB2. 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.