Rare genetic neurological disorder Familial exudative vitreoretinopathy OMIM:133780 MESH:C536382 orphanet OMIM:613310 OMIM:605750 ICD10:H35.0 UMLS:C1851402 OMIM:305390 Criswick-Schepens syndrome UMLS:C0339539 OMIM:616468 OMIM:617572 FEVR Familial exudative vitreoretinopathy (FEVR) is a rare hereditary vitreoretinal disorder characterized by abnormal or incomplete vascularization of the peripheral retina leading to variable clinical manifestations ranging from no effects to minor anomalies, or even retinal detachment with blindness. OMIM:601813 Genetic vitreous-retinal disease