Disease Info Card

Congenital Abnormality

Information about Congenital Abnormality: 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 Congenital Abnormality

Most recent studies have shown that Congenital Abnormality shares some biological mechanisms with atresia, cleft-lip, cleft-palate, congenital-absence, congenital-heart-defects, cytogenetic-abnormality, diabetes-mellitus, dysplasia, fetal-death, fetal-diseases, fracture, gonadal-dysgenesis, hypoplasia, malignant-neoplasms, neoplasms, nervousness, pain, pregnancy-complications.

Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Abnormality, and have been seen in publications frequently: Aging, Brain Development, Cell Cycle, Cell Death, Cell Proliferation, Excretion, Fertilization, Localization, Methylation, Ossification, Ovulation, Pathogenesis, Regeneration, Secretion, Segmentation, Spermatogenesis, Translation, Transport, Transposition, Wound Healing

Quite a number of genes have been found to play important roles in Congenital Abnormality, such as AFP, AR, BEST1, BRD2, CAT, CP, CSF2, DMD, FANCA, INS, NDUFB6, NR5A1, PES1, SHH, SRY, SS18L1, TNF. 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.

Congenital Abnormality Related Genes

click to see detail information for each gene

AFP AR BEST1
BRD2 CAT CP
CSF2 DMD FANCA
INS NDUFB6 NR5A1
PES1 SHH SRY
SS18L1 TNF