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Disease Info Card
Avellino Corneal Dystrophy
Information about Avellino Corneal Dystrophy: 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 Avellino Corneal Dystrophy
Most recent studies have shown that Avellino Corneal Dystrophy shares some biological mechanisms with amyloidosis, blind-vision, corneal-deposits, corneal-diseases, corneal-dystrophy-lattice-type-3, dystrophy, familial-amyloid-polyneuropathy-type-v, granular-corneal-dystrophy, hereditary-corneal-dystrophy, myopia, photophobia, plaque-amyloid, pyotraumatic-dermatitis, recurrence-(disease-attribute), reis-bucklers-corneal-dystrophy, stromal-corneal-dystrophy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Avellino Corneal Dystrophy, and have been seen in publications frequently: Autophagy, Cell Cycle, Cell Death, Cell Growth, Localization, Pathogenesis, Secretion, Wound Healing
Quite a number of genes have been found to play important roles in Avellino Corneal Dystrophy, such as ACD, CHST6, FMN1, GCDH, GSR, NLGN1, PARP1, PLK3, PPP1R1A, PSMD1, PTK2B, RPS6KB2, SMAD3, SQSTM1, TGFB1, TGFBI, ZAP70. 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 Avellino Corneal Dystrophy
This information is being compiled and will come in a future update
| Autophagy | Cell Cycle | Cell Death |
| Cell Growth | Localization | Pathogenesis |
| Secretion | Wound Healing |