Weaver syndrome
Sotos syndrome
Carpenter syndrome
Treacher Collins syndrome
Hallermann-Streiff syndrome
embryofetopathy
Edwards syndrome
trisomy 21
Down syndrome
Beckwith-Wiedemann syndrome
embryopathy
Down's syndrome
mongolism
mongolianism
Noonan syndrome
Cockayne syndrome
Wolf-Hirschhorn syndrome
Nijmegen breakage syndrome
Crouzon syndrome
Timothy syndrome
Pallister-Hall syndrome
lipochondrodystrophy
macroencephaly
Hurler's syndrome
Hurler's disease
dysostosis multiplex
gargoylism
macrencephaly
Johanson-Blizzard syndrome
Proteus syndrome
Seckel syndrome
adermatoglyphia
FG syndrome
dwarfism
Pfeiffer syndrome
nanism
meiogynogenetic
hereditary hemorrhagic telangiectasia
pregenitally
mutable
neuroteratological
Dubowitz syndrome
oligophrenia
Bloom's syndrome
Dravet syndrome
hypogenesis
achondroplasty
microhydranencephaly
achondroplasia
embryopathological
Cornelia de Lange syndrome
acephalocheiria
ablepharon macrostomia syndrome
Schinzel-Giedion syndrome
chondrodysplasia
osteosclerosis congenita
neurobehavior
neuromere
Batten disease
chondrodystrophy
organic defect
pycnodysostosis
geneagenetic
Camurati-Engelmann disease
ameiotic
pregenitality
natural
Börjeson–Forssman–Lehmann syndrome
arrested development
premutative
embryopathology
Landau-Kleffner syndrome
neurogenetics
cranioschisis
pontocerebellar hypoplasia
idiogenetic
Feingold syndrome
regression
Pascual-Castroviejo syndrome type 1
fixation
infantile fixation
chromoanagenetic
holoprosencephaly
malformation
neotenic complex syndrome
chromogenetic
progeria
dysmorphology
epimorphotic
piebaldism
premenstrual stress
mutagenesis
excrescent
teratoid
Williams syndrome
embryopathic
congenital
melorheostosis

English words for 'A rare autosomal-dominant genetic disorder associated with rapid growth beginning in the prenatal period, characterized by advanced osseous maturation and distinctive craniofacial, skeletal and neurological abnormalities.'

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