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Disease Info Card
Zimmermann-laband Syndrome
Information about Zimmermann-laband 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 Zimmermann-laband Syndrome
Most recent studies have shown that Zimmermann-laband Syndrome shares some biological mechanisms with anterior-open-bite, chromosome-breakage, congenital-foot-deformity, congenital-hand-deformities, craniofacial-abnormalities, cytogenetic-abnormality, dysplasia, epilepsy, fibromatosis, fibromatosis-gingival, gingival-hyperplasia, hyperplasia, hypertrichosis, hypertrophy, hypoplasia, nails-malformed, tooth-supernumerary.
Among the many pathways, these few ones have gauged particular interests from scientists studying Zimmermann-laband Syndrome, and have been seen in publications frequently: Keratinization, Tooth Eruption
Quite a number of genes have been found to play important roles in Zimmermann-laband Syndrome, such as CACNA2D1, CACNA2D3, CDK2AP2, CDKN1A, CDKN2A, ENDOU, ERC2, EXOSC6, INS, LAMTOR2, LRTM1, NSG1, S100A10, S100A9, SUB1, TCEAL1, WNT5A. 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 Zimmermann-laband Syndrome
This information is being compiled and will come in a future update
| Keratinization | Tooth Eruption |