Laurence-Moon syndrome
Lowe syndrome
Miller syndrome
Aicardi syndrome
Bardet-Biedl syndrome
retinopathology
Keutel syndrome
reticulohistiocytosis
GAPO syndrome
preretinopathy
pachydermoperiostosis
incontinentia pigmenti
Wolf-Hirschhorn syndrome
Pfeiffer syndrome
Joubert syndrome
bestrophinopathy
CHARGE syndrome
retinopathic
neuroretinopathy
livedo racemosa
ablepharon macrostomia syndrome
retinoblastoma protein
hypodicrotic
reticulopodial
nail-patella syndrome
reticulocytotic
reticulocytopenic
retinophoral
Pallister-Hall syndrome
Weill-Marchesani syndrome
idiotism
Schinzel-Giedion syndrome
Feingold syndrome
retinosis
retinoschisis
Norrie disease
retinopathy
diseasome
RIDDLE syndrome
retinochoroidopathy
Dubowitz syndrome
keratosis blennorrhagica
reticulo-
Langer-Giedion syndrome
adermatoglyphia
visuotopic
retinocytoma
Townes-Brocks syndrome
Bart syndrome
keratoderma blennorrhagica
Berk-Tabatznik syndrome
cross wires
3C syndrome
Urbach-Wiethe disease
Charcot-Marie-Tooth
dysostosis multiplex
Hurler's syndrome
Bayoud disease
lipochondrodystrophy
abducens oculi
Hurler's disease
syphilitically
Aicardi-Goutières syndrome
retardation
palindromia
gargoylism
reticuloruminal
Reiter's disease
Reiter's arthritis
Allan-Herndon-Dudley syndrome
adarotene
fragile X syndrome
pathogenetics
retardive
onychopathic
polychromia
retinitis
FG syndrome
retinoblastoma
reticled
reticuloid
retinogenic
retinoscopic
microangiopathological
cartilage-hair hypoplasia
dyscromia
genetic disorder
Mendes da Costa syndrome
muscle-eye-brain disease
retinotoxicity
Marshall syndrome
Baller-Gerold syndrome
faciodigitogenital dysplasia
retinochoroidal
hypostrophe
Marinesco-Sjögren syndrome
paraneoplasia
yellow nail syndrome
Cornelia de Lange syndrome

English words for 'A rare genetic disorder associated with retinitis pigmentosa, extra digits, spastic paraplegia, hypogonadism, and mental retardation.'

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