Acquired Color Blindness

Acquired Color Blindness, also known as acquired colour vision deficiencies, is related to intraocular pressure quantitative trait locus and axenfeld-rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities. An important gene associated with Acquired Color Blindness is NXNL1 (Nucleoredoxin Like 1), and among its related pathways/superpathways are Mesodermal commitment pathway and Prostaglandin synthesis and regulation. Affiliated tissues include eye and prostate, and related phenotypes are Decreased viability with carboplatin and nervous system