Keutel syndrome
faciodigitogenital dysplasia
Meckel-Gruber syndrome
Baller-Gerold syndrome
Laurence-Moon syndrome
chondrodystrophia
chondrodystrophy
CHARGE syndrome
Joubert syndrome
Townes-Brocks syndrome
ablepharon macrostomia syndrome
Langer-Giedion syndrome
Weill-Marchesani syndrome
hypertrichosis
RIDDLE syndrome
Carpenter syndrome
Feingold syndrome
dysostosis multiplex
chondropathy
Maffucci syndrome
Hurler's disease
Hurler's syndrome
Pallister-Hall syndrome
lipochondrodystrophy
gargoylism
polychondritis
Aicardi syndrome
Farber disease
incontinentia pigmenti
Urbach-Wiethe disease
cartilage-hair hypoplasia
Cornelia de Lange syndrome
pachydermoperiostosis
Wolf-Hirschhorn syndrome
subcartilaginous
POEMS syndrome
Bonnet-Dechaume-Blanc syndrome
Pfeiffer syndrome
3C syndrome
cartilaginification
Larsen syndrome
hydroanencephalic
Bardet-Biedl syndrome
Cowden syndrome
Pierre Robin sequence
nail-patella syndrome
genetic disorder
cartilaginous
nanocephaly
Milroy's disease
Babylonic
pseudolesion
Ollier disease
dysplastic
cystopathic
Costello syndrome
Fanconi anemia
trichopathic
semicartilaginous
supranuclear palsy
cephalopolysyndactyly
chondropathic
spondyloenchondrodysplasia
ovalocytotic
Miller syndrome
uta
laryngotracheobronchopneumonitis
precartilaginous
muscle-eye-brain disease
chondroectodermal
oriental sore
cricovocal
laryngotracheobronchitis
Treacher Collins syndrome
phocomelia
Bartter syndrome
hypochondrodysplasia
piebaldism
acheiropody
Lowe syndrome
Kienbock's disease
macrocephaly
cytopathologically
path
acrodysplasia
Hartnup disorder
GAPO syndrome
cytopathically
Marshall syndrome
Dubowitz syndrome
Bart syndrome
adenocele
chytridiosis
zonulopathy
Léri-Weill dyschondrosteosis
reticulohistiocytosis
Chédiak-Higashi syndrome
Leri's pleonosteosis

English words for 'A rare genetic disorder characterized by abnormal diffuse cartilage calcification, hypoplasia of the mid-face, peripheral pulmonary stenosis, hearing loss, short distal phalanges of the fingers, and mild mental retardation.'

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