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Disease Info Card
Cryptorchidism
Information about Cryptorchidism: 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 Cryptorchidism
Most recent studies have shown that Cryptorchidism shares some biological mechanisms with atrophy, congenital-abnormality, disorders-of-sex-development, dysgerminoma, hernia, hernia-inguinal, hypogonadism, hypospadias, infertility, male-infertility, malignant-neoplasm-of-testis, malignant-neoplasms, neoplasms, seminoma, testicular-diseases, testicular-neoplasms, undescended-testes---bilateral, unilateral-undescended-testis, varicocele.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cryptorchidism, and have been seen in publications frequently: Cell Death, Cell Development, Cell Differentiation, Cell Maturation, Cell Proliferation, Excretion, Fertilization, Germ Cell Development, Gonadotropin Secretion, Localization, Mating, Meiosis, Pathogenesis, Secretion, Sex Differentiation, Sperm Motility, Spermatogenesis, Testosterone Secretion, Transport, Transposition
Quite a number of genes have been found to play important roles in Cryptorchidism, such as AKR1B1, AMH, AR, AREG, BRD2, CGA, ESR1, FDXR, GNRH1, INSL3, NR5A1, PLOD1, POMC, PRL, RXFP2, SHBG. 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.