Lowe syndrome
Norrie disease
Wolf-Hirschhorn syndrome
Pfeiffer syndrome
Aicardi syndrome
Weill-Marchesani syndrome
CHARGE syndrome
retinosis
Laurence-Moon syndrome
Marinesco-Sjögren syndrome
Berk-Tabatznik syndrome
GAPO syndrome
Norrie
neuroretinopathy
micropolygyria
Dubowitz syndrome
Waardenburg syndrome
mongolism
Timothy syndrome
Down's syndrome
Cornelia de Lange syndrome
retinoschisis
Pascual-Castroviejo syndrome type 1
Down syndrome
Pallister-Hall syndrome
Marshall syndrome
mongolianism
trisomy 21
Aicardi-Goutières syndrome
choroideremia
Nijmegen breakage syndrome
Baller-Gerold syndrome
FG syndrome
Schinzel-Giedion syndrome
metamorphopsia
retinopathology
Bálint's syndrome
Miller syndrome
genetic disorder
Duane syndrome
Charcot-Marie-Tooth
bestrophinopathy
ablepharon macrostomia syndrome
adermatoglyphia
neurogenetics
3C syndrome
neurodisorder
preretinopathy
blind
Börjeson–Forssman–Lehmann syndrome
idiotism
Townes-Brocks syndrome
Brown syndrome
Moebius syndrome
retinopathy
Carpenter syndrome
Leigh disease
Brunner syndrome
Joubert syndrome
incontinentia pigmenti
Allan-Herndon-Dudley syndrome
Edwards syndrome
RCS rat
retinitis pigmentosa
simple hyperopia
aniseikonic
Treacher Collins syndrome
ametropia
glaucoma
optic cup
Usher syndrome
monosomy
myotonic dystrophy
drusen
cartilage-hair hypoplasia
fragile X syndrome
Stickler syndrome
eyecup
mixed astigmatism
hereditary hemorrhagic telangiectasia
compound hyperopia
muscle-eye-brain disease
neuroanalysis
point mutation
Feingold syndrome
mutable
Costello syndrome
retinoblastoma protein
Tay-Sachs disease
gene mutation
hypomorphism
nervous disorder
Noonan syndrome
simple myopia
astigmatism
neurological disease
supranuclear palsy
retinopathic
neurological disorder