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Disease Info Card
Hypoplasia Of Scrotum
Information about Hypoplasia Of Scrotum: 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 Hypoplasia Of Scrotum
Most recent studies have shown that Hypoplasia Of Scrotum shares some biological mechanisms with congenital-abnormality, congenital-clubfoot, congenital-foot-deformity, cryptorchidism, cytogenetic-abnormality, developmental-delay-(disorder), dwarfism, dysplasia, flexed-fetal-attitude, growth-retardation, hernia, hypoplasia, hypospadias, microcephaly, micrognathism, muscle-hypotonia, penis-agenesis, trisomy, undescended-testes---bilateral.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hypoplasia Of Scrotum, and have been seen in publications frequently: Glycosylation, Limb Development, Ossification, Pigmentation
Quite a number of genes have been found to play important roles in Hypoplasia Of Scrotum, such as ALX3, BRD2, CDK2AP2, CDKN2A, CDKN2B, DCTN3, DYNC1H1, GLI3, INVS, LMLN, MRPL28, NXT1, PAX6, PLOD1, SRY, SUB1, 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.
Pathways Related to Hypoplasia Of Scrotum
This information is being compiled and will come in a future update
| Glycosylation | Limb Development | Ossification |
| Pigmentation |