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Disease Info Card
Congenital Funnel Chest
Information about Congenital Funnel Chest: 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 Congenital Funnel Chest
Most recent studies have shown that Congenital Funnel Chest shares some biological mechanisms with blepharoptosis, congenital-abnormality, congenital-heart-defects, congenital-pectus-carinatum, depressive-disorder, dyspnea, heart-diseases, hemorrhage, hernia, hypoplasia, lung-diseases, marfan-syndrome, mitral-valve-prolapse-syndrome, pain, pain-postoperative, pathological-dilatation, scoliosis-unspecified, stenosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Funnel Chest, and have been seen in publications frequently: Aging, Blood Circulation, Chondrocyte Proliferation, Coagulation, Dehiscence, Endochondral Ossification, Excretion, Hemostasis, Localization, Lung Growth, Muscle Contraction, Myelination, Ossification, Oxygen Transport, Pathogenesis, Regeneration, Swimming, Transport, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Congenital Funnel Chest, such as ADRB2, AP3B1, BFAR, CAT, CRAT, CTBP1, FBN1, FEV, FLVCR1, GLYAT, GPSM2, KRAS, NDUFB6, NR1H4, PES1, PREP, PTCH1, RANGAP1. 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.