vitreous disorder persistent hyperplastic primary vitreous https://www.malacards.org/card/persistent_hyperplastic_primary_vitreous persistent fetal vasculature syndrome MEDGEN:120583 MONDO:0019631 DOID:0060282 SCTID:314270008 OMIMPS:221900 GARD:0016803 NCIT:C161554 persistent foetal vasculature syndrome Orphanet:91495 PHPV non-syndromic congenital retinal non-attachment PFVS congenital retinal detachment A developmental ocular anomaly in which the primary vitreous body and its surrounding hyaloid vasculature failed to regress. It is usually unilateral and characterized by cataract; microphthalmos (small eyeballs), and retrolenticular fibrovascular tissue. (from Yanoff: Ophthalmology, 2nd ed.) MESH:D054514 icd11.foundation:1011137326 UMLS:C0266568 ncRNA disease congenital vitreoretinal dysplasia