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Disease Info Card
Congenital Coloboma Of Iris
Information about Congenital Coloboma Of Iris: 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 Coloboma Of Iris
Most recent studies have shown that Congenital Coloboma Of Iris shares some biological mechanisms with atresia, atrophy, blepharoptosis, cataract, cleft-palate, congenital-abnormality, congenital-heart-defects, congenital-ocular-coloboma-(disorder), corneal-diseases, dysplasia, eye-abnormalities, glaucoma, hypoplasia, iris-diseases, microcephaly, microphthalmos, orbital-separation-excessive, strabismus.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Coloboma Of Iris, and have been seen in publications frequently: Amelogenesis, Coagulation, Conjugation, Dehiscence, Eye Development, Eye Morphogenesis, Glycosylation, Innervation, Myelination, Pathogenesis, Pigmentation, Transposition
Quite a number of genes have been found to play important roles in Congenital Coloboma Of Iris, such as BRCA1, CAT, CHD7, CKAP4, CRAT, CRYAA, GLYAT, IKBKG, INVS, LMLN, MAF, MRPL28, PAX6, PQBP1, SS18L1, TNFSF14. 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 Congenital Coloboma Of Iris
This information is being compiled and will come in a future update
| Amelogenesis | Coagulation | Conjugation |
| Dehiscence | Eye Development | Eye Morphogenesis |
| Glycosylation | Innervation | Myelination |
| Pathogenesis | Pigmentation | Transposition |