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Disease Info Card
Lipoid Proteinosis Of Urbach And Wiethe
Information about Lipoid Proteinosis Of Urbach And Wiethe: 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 Lipoid Proteinosis Of Urbach And Wiethe
Most recent studies have shown that Lipoid Proteinosis Of Urbach And Wiethe shares some biological mechanisms with brain-diseases, calcinosis, cicatrix, dermatologic-disorders, disorders-of-porphyrin-metabolism, fibrosis, hereditary-diseases, hoarseness, hyalinization, laryngeal-diseases, lipoidosis, lung-diseases, mouth-diseases, mucinous-adenocarcinoma, pneumonia, pulmonary-alveolar-proteinosis, pulmonary-fibrosis, respiratory-tract-diseases, skin-diseases-genetic.
Among the many pathways, these few ones have gauged particular interests from scientists studying Lipoid Proteinosis Of Urbach And Wiethe, and have been seen in publications frequently: Anaphylaxis, Angiogenesis, Blood Coagulation, Cognition, Fibroblast Proliferation, Granuloma Formation, Humoral Immune Response, Hypersensitivity, Immune Response, Keratinocyte Differentiation, Lipid Storage, Localization, Lymphangiogenesis, Menopause, Methylation, Pathogenesis, Pigmentation, Secretion, Translation, Wound Healing
Quite a number of genes have been found to play important roles in Lipoid Proteinosis Of Urbach And Wiethe, such as ALB, CCL2, COL1A2, ECM1, EFEMP1, FECH, FN1, IL13, INS, LPA, LYVE1, MBL2, SEPSECS, SFTPC, SFTPD, SMPD1, TNF. 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.