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Disease Info Card
Congenital Absence Of Spleen
Information about Congenital Absence Of Spleen: 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 Absence Of Spleen
Most recent studies have shown that Congenital Absence Of Spleen shares some biological mechanisms with accessory-spleen, anemia, anemia-sickle-cell, anomalous-pulmonary-venous-connection, atresia, bacterial-infections, bilateral-right-sidedness-sequence, congenital-abnormality, congenital-absence, congenital-heart-defects, congenital-heart-disease, heart-diseases, infective-disorder, pneumococcal-infections, pneumonia, situs-ambiguus, situs-inversus, splenic-diseases, systemic-infection.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Absence Of Spleen, and have been seen in publications frequently: Adaptive Immune Response, Aging, Cell Death, Coagulation, Complement Activation, Exogen, Hypersensitivity, Immune Response, Liver Development, Localization, Ossification, Pathogenesis, Phagocytosis, Programmed Cell Death, Reflex, Regeneration, Response To Lipopolysaccharide, Segmentation, Spleen Development, Transposition
Quite a number of genes have been found to play important roles in Congenital Absence Of Spleen, such as AMY2A, BLOC1S6, BMP4, C3, CD8A, CFP, CSF2, EPB42, HMOX1, LAMC2, NKX3-2, PRH1, SCD, TLX1. 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.