Urethral Meatus Stenosis

Overview of Urethral Meatus Stenosis

Most recent studies have shown that Urethral Meatus Stenosis shares some biological mechanisms with acquired-phimosis, balanitis, balanitis-xerotica-obliterans, cicatrix, congenital-abnormality, diverticulum, gastroesophageal-reflux-disease, hemorrhage, hypospadias, lichen-sclerosus-et-atrophicus, pathologic-fistula, pathological-dilatation, stenosis, urethral-diseases, urethral-fistula, urethral-stricture, urinary-fistula, urinary-tract-infection.

Among the many pathways, these few ones have gauged particular interests from scientists studying Urethral Meatus Stenosis, and have been seen in publications frequently: Aging, Dehiscence, Enucleation, Hemostasis, Inflammatory Response, Liver Development, Localization, Menopause, Micturition, Pathogenesis, Penile Erection, Pigmentation, Regeneration, Transposition, Wound Healing

Quite a number of genes have been found to play important roles in Urethral Meatus Stenosis, such as ACAT1, ALOX5AP, GNL3, HES1, HMGCL, HMOX1, ITFG1, KAT5, KRAS, LIPC, PTGDS, RANGAP1, SALL1, SLC17A5, SLC25A5, SLC26A4, TIPRL. 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.

Urethral Meatus Stenosis Related Genes

click to see detail information for each gene

Pathways Related to Urethral Meatus Stenosis

This information is being compiled and will come in a future update

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