Preferred Label : Goldmann-Favre syndrome;
ICD-11 definition : Goldmann-Favre syndrome is a genetic vitreoretinal dystrophy characterized by early
onset of night blindness, reduced bilateral visual acuity, and typical fundus findings
(progressive pigmentary degenerative changes, macular edema, retinoschisis).;
Origin ID : 890235941;
Automatic exact mappings (from CISMeF team)
Goldmann-Favre syndrome is a genetic vitreoretinal dystrophy characterized by early
onset of night blindness, reduced bilateral visual acuity, and typical fundus findings
(progressive pigmentary degenerative changes, macular edema, retinoschisis).
