GAPO syndrome
Berk-Tabatznik syndrome
Miller syndrome
Lowe syndrome
CHARGE syndrome
ametropia
incontinentia pigmenti
Laurence-Moon syndrome
Norrie disease
cartilage-hair hypoplasia
Weill-Marchesani syndrome
Duane syndrome
Proteus syndrome
preretinopathy
retinopathology
ophthalmopathic
pachydermoperiostosis
pseudoxanthoma elasticum
Cornelia de Lange syndrome
mongolianism
Down's syndrome
Brown syndrome
mongolism
Down syndrome
Marshall syndrome
trisomy 21
keratopathy
Pfeiffer syndrome
maculopathy
Baller-Gerold syndrome
alopecian
oculopathy
Dubowitz syndrome
ablepharon macrostomia syndrome
glaucoma
adermatoglyphia
onychopathic
ophthalmopathy
Langer-Giedion syndrome
dermatoporosis
atrophied
Waardenburg syndrome
neuroretinopathy
Börjeson–Forssman–Lehmann syndrome
cryptophthalmos
Marinesco-Sjögren syndrome
Costello syndrome
retinosis
odd-eyed
choroideremia
ichthyosis hystrix
iridopathy
atrogenic
aniridia
faciodigitogenital dysplasia
brittle bone disease
retinitis pigmentosa
Cowden syndrome
alopecic
Treacher Collins syndrome
Léri-Weill dyschondrosteosis
bestrophinopathy
Feingold syndrome
glass bone disease
hypochondroplasia
Wolf-Hirschhorn syndrome
RIDDLE syndrome
trichomegaly
lenticonus
Urbach-Wiethe disease
mutagen
Bart syndrome
nail-patella syndrome
xeroderma pigmentosum
dysostosis multiplex
Martin-Albright syndrome
FG syndrome
polychromia
Hurler's syndrome
lipochondrodystrophy
athetoid
Pascual-Castroviejo syndrome type 1
gargoylism
Hurler's disease
kirat
pathomorphogenic
Sebright bantam syndrome
Schinzel-Giedion syndrome
Aicardi syndrome
dry eye
Stargardt disease
pseudolesion
microspherophakia
acomia
Bálint's syndrome
cataract
Noonan syndrome
ablepharia
Keutel syndrome

English words for 'A rare genetic disorder characterized by growth retardation, alopecia, pseudoanodontia, and progressive optic atrophy.'

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