NEO1, neogenin 1, 4756

N. diseases: 52; N. variants: 0
Disease: Blindness ×
Source: BEFREE ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0456909
Disease: Blindness
Blindness 		0.010 Biomarker phenotype BEFREE Here we present evidence that loss of neogenin contributes to pathogenesis of persistent hyperplastic primary vitreous formation (PHPV), a genetic disorder accounting for ~5% of blindness in the USA (United States of America). 31336386 2020