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Disease Info Card
Anorectal Anomaly
Information about Anorectal Anomaly: 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 Anorectal Anomaly
Most recent studies have shown that Anorectal Anomaly shares some biological mechanisms with anus-imperforate, atresia, congenital-abnormality, congenital-absence, congenital-digestive-system-anomalies, constipation, currarino-triad, fecal-incontinence, hirschsprung-disease, intestinal-obstruction, pathologic-fistula, pathological-dilatation, rectal-fistula, rectourethral-fistula, rectovaginal-fistula, spina-bifida, stenosis, urethral-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Anorectal Anomaly, and have been seen in publications frequently: Cell Adhesion, Defecation, Dehiscence, Embryo Development, Fertilization, Granuloma Formation, Hemostasis, Innervation, Localization, Menstruation, Micturition, Ossification, Pathogenesis, Proprioception, Reflex, Response To Histamine, Segmentation, Transport, Transposition, Wound Healing
Quite a number of genes have been found to play important roles in Anorectal Anomaly, such as ABCC6, ACE, ACHE, CS, DACT1, FGF10, FOXC1, GNAI1, HTT, MNX1, MYOG, PSMD3, RANGAP1, SLC17A5, SLC7A5, TAOK1, TMEFF2, WNT5A. 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.