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Disease Info Card
Essential Fatty Acid Deficiency
Information about Essential Fatty Acid Deficiency: 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 Essential Fatty Acid Deficiency
Most recent studies have shown that Essential Fatty Acid Deficiency shares some biological mechanisms with cholestasis, cystic-fibrosis, deficiency-diseases, dermatitis, dermatologic-disorders, diabetes-mellitus, fatty-liver, fibrosis, glomerulonephritis, growth-retardation, hyperplasia, inflammation, liver-diseases, malabsorption-syndrome, malnutrition, neoplasms, nutrition-disorders, protein-energy-malnutrition, zinc-deficiency-disorder.
Among the many pathways, these few ones have gauged particular interests from scientists studying Essential Fatty Acid Deficiency, and have been seen in publications frequently: Brain Development, Cell Adhesion, Cell Proliferation, Chemotaxis, Cholesterol Esterification, Coagulation, Excretion, Glomerular Filtration, Immune Response, Inflammatory Response, Lactation, Lipid Transport, Mating, Myelination, Oxidative Phosphorylation, Pathogenesis, Platelet Aggregation, Secretion, Transport, Wound Healing
Quite a number of genes have been found to play important roles in Essential Fatty Acid Deficiency, such as ALB, CD19, CFTR, CSH1, DBT, FANCA, FXN, HOXA10, INS, LPL, PLEKHM1, PNLIP, PREP, TEAD1, TG, TIMP1, 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.