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- Table of Contents
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Disease Info Card
Failure To Thrive
Information about Failure To Thrive: 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 Failure To Thrive
Most recent studies have shown that Failure To Thrive shares some biological mechanisms with acidosis, anemia, congenital-abnormality, developmental-delay-(disorder), developmental-disabilities, diarrhea, fibrosis, gastroesophageal-reflux-disease, growth-disorders, growth-retardation, immunologic-deficiency-syndromes, infective-disorder, malabsorption-syndrome, malnutrition, muscle-hypotonia, pain, pneumonia, vomiting.
Among the many pathways, these few ones have gauged particular interests from scientists studying Failure To Thrive, and have been seen in publications frequently: Aging, Brain Development, Cell Proliferation, Coagulation, Dna Repair, Excretion, Fatty Acid Oxidation, Gastric Emptying, Glomerular Filtration, Glycosylation, Hypersensitivity, Lactation, Localization, Myelination, Oxidative Phosphorylation, Pathogenesis, Pigmentation, Reflex, Secretion, Transport
Quite a number of genes have been found to play important roles in Failure To Thrive, such as ADA, CD4, CFTR, CSF2, CYCS, CYP11B2, GGH, GH1, GLB1, HRAS, IGF1, INS, MAP2K1, MAP2K2, NR3C2, POMC, REN, TCN2. 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.