Hurler's disease
dysostosis multiplex
lipochondrodystrophy
gargoylism
Hurler's syndrome
Carpenter syndrome
faciodigitogenital dysplasia
chondrodystrophy
ablepharon macrostomia syndrome
Baller-Gerold syndrome
inborn error of metabolism
Marfan's syndrome
osteosclerosis congenita
achondroplasia
Feingold syndrome
achondroplasty
Camurati-Engelmann disease
adermatoglyphia
Treacher Collins syndrome
osteochondrodysplasia
Bardet-Biedl syndrome
nail-patella syndrome
Weaver syndrome
Cowden syndrome
Timothy syndrome
pachydermoperiostosis
Salla disease
Bart syndrome
osteodystrophy
acheiropody
methylmalonic acidemia
Keutel syndrome
Miller syndrome
Edwards syndrome
histidinemia
Zellweger syndrome
dysostosis
luxoid
microspecies
Niemann-Pick disease
dysosteosclerosis
Rett syndrome
autophagocytosed
autogynephilic
clinodactyly
aetiopathogenesis
polyarthropathy
opsismodysplasia
mutagenic
Townes-Brocks syndrome
pathogenetics
metabola
plurimetabolic
enzymopathy
dyschondrosteosis
ectrodactyly
osteogenesis imperfecta
mutagenize
oligodactyly
genetic abnormality
hereditary hemorrhagic telangiectasia
osteopetrosis
chondrodystrophia
genetic defect
inherited disorder
genetic disorder
congenital disease
ketoacidemia
Börjeson–Forssman–Lehmann syndrome
mutate
inherited disease
Costello syndrome
hereditary condition
onychopathic
genetic disease
mutative
hereditary disease
phocomelia
polyposis
Lambert-Eaton myasthenic syndrome
metabolic disorder
metabolopathy
pathomorphosis
Pascual-Castroviejo syndrome type 1
distal muscular dystrophy
apomeiotic
autotomic
mutating
pathological
cytodegenerative
Bartter syndrome
pathosis
genodermatose
pathogenesis
symbrachydactyly
idiopathic disease
mutatory
idiopathic disorder

English words for 'hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skeletal cartilage and bone and mental retardation'

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