This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Optic Nerve Hypoplasia
Information about Optic Nerve Hypoplasia: 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 Optic Nerve Hypoplasia
Most recent studies have shown that Optic Nerve Hypoplasia shares some biological mechanisms with atrophy, blind-vision, congenital-abnormality, congenital-ocular-coloboma-(disorder), diabetes-mellitus, disorder-of-eye, disorder-of-the-optic-nerve, dysplasia, eye-abnormalities, hypopituitarism, hypoplasia, microphthalmos, nervousness, nystagmus, optic-atrophy, pituitary-diseases, septo-optic-dysplasia, strabismus, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Optic Nerve Hypoplasia, and have been seen in publications frequently: Axon Guidance, Brain Development, Cell Death, Cell Development, Cell Migration, Developmental Process, Fertilization, Glycosylation, Growth Hormone Secretion, Hormone Secretion, Localization, Myelination, Nerve Development, Optic Nerve Development, Pathogenesis, Pigmentation, Protein Glycosylation, Reflex, Secretion, Spermatogenesis
Quite a number of genes have been found to play important roles in Optic Nerve Hypoplasia, such as AKR1C2, ATP2A2, AVP, ERG, GGH, GH1, GHRH, HES1, HESX1, KCNH2, NTN1, OPN1LW, PAX6, POMC, PRL, SOD1. 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.