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Disease Info Card
Mayer-rokitansky-kuster-hauser Syndrome
Information about Mayer-rokitansky-kuster-hauser Syndrome: 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 Mayer-rokitansky-kuster-hauser Syndrome
Most recent studies have shown that Mayer-rokitansky-kuster-hauser Syndrome shares some biological mechanisms with abdominal-pain, amenorrhea, aplasia-nos, atresia, atresia-of-vagina, blepharoptosis, congenital-abnormality, congenital-absence, congenital-absence-of-kidney, dysplasia, gonadal-dysgenesis, hemorrhage, neoplasms, pain, pathological-dilatation, primary-physiologic-amenorrhea, stenosis, urogenital-abnormalities, uterine-agenesis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mayer-rokitansky-kuster-hauser Syndrome, and have been seen in publications frequently: Cell Growth, Development Of Secondary Sexual Characteristics, Fertilization, Innervation, Kidney Morphogenesis, Limb Development, Localization, Menarche, Menstruation, Metaphase, Methylation, Oocyte Development, Ovulation, Pathogenesis, Secretion, Thelarche, Transposition
Quite a number of genes have been found to play important roles in Mayer-rokitansky-kuster-hauser Syndrome, such as ASAP1, BBS2, CS, FGF2, GALT, HNF1B, HOXA13, LHX1, MKKS, MKS1, PAPOLA, PDAP1, RARG, REG3A, TUSC2, WNT4, WT1. 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.