Ackerman syndrome
Wyburn-Mason syndrome
syndromically
spasmus nutans
Weill-Marchesani syndrome
genodermatotic
Opitz-Kaveggia syndrome
Hailey-Hailey disease
cherubism
Fahr disease
Bernard-Horner syndrome
Claude Bernard-Horner syndrome
Claude Bernard syndrome
Cornelia de Lange syndrome
syndromic
Pashayan syndrome
genodermatose
prostitute's pupil
Timothy syndrome
merycism
keratopathy
Noonan's syndrome
syndromal
eye disease
Léri-Weill dyschondrosteosis
keratoconjunctivitis sicca
hyperdicrotism
frontated
syndromics
CHARGE syndrome
hyperthermophilicity
hyperthermophily
Hashimoto-Pritzker disease
anisocoria
oligodendrogliopathy
microstomia
pseudopit
agangliosis
Urbach-Wiethe disease
myotonic dystrophy
hypermetamorphotic
familistic
macrocephalic
nephrotic syndrome
Allgrove syndrome
Cowden syndrome
glomerulopenia
zonulopathy
nephrosis
folliculotropism
Cotard delusion
Florence syndrome
macrencephaly
Berk-Tabatznik syndrome
Pfeiffer syndrome
Flammer syndrome
ablepharia
achondroplasia
albinism
Nager acrofacial dysostosis
Rasmussen syndrome
Aarskog-Scott syndrome
poikiloderma congenitale
Marfan's syndrome
Kallman syndrome
tongue-tie
microtropia
hypospermatogenetic
hyperpigmented
teratism
ophthalmopathy
multilesion
maculopathy
basophilia
faciocutaneoskeletal
Pascual-Castroviejo syndrome type 1
microstrabismus
Carpenter syndrome
aniridia
horsetail syndrome
ichthyosis bullosa of Siemens
oculopathy
onychopathic
scleroatrophy
palaeoclimatologic
isocoria
chondropathic
Turner's syndrome
hyperpyretic
pinocytotic
Klüver-Bucy syndrome
Neill-Dingwall syndrome
gyrotrigonometric
palaeoclimatological
capillaropathic
palsied
dyscoria
fibroglycemia
Klippel-Trénaunay-Weber syndrome
Weber-Cockayne syndrome

English words for 'A familial syndrome characterised by taurodontism, hypotrichosis, full upper lip without a Cupid's bow, thickened and wide philtrum, and occasional juvenile glaucoma.'

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