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Congenital disease
/kəndʒˈɛnətəl
dɪzˈiz/
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Congenital disease
noun
1.
A disease or disorder that is inherited genetically.
Synonyms:
genetic abnormality
,
genetic defect
,
genetic disease
,
genetic disorder
,
hereditary condition
,
hereditary disease
,
inherited disease
,
inherited disorder
.
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Etymology of 'Congenital disease'
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Words linked to "Congenital disease" :
genetic disorder
,
genetic disease
,
Fanconi's anemia
,
Albers-Schonberg disease
,
achondroplasia
,
achondroplasty
,
polygenic disorder
,
inherited disease
,
marble bones disease
,
hepatolenticular degeneration
,
autosomal dominant disorder
,
inherited disorder
,
chondrodystrophy
,
autosomal recessive defect
,
branched chain ketoaciduria
,
Spielmeyer-Vogt disease
,
maple syrup urine disease
,
muscular dystrophy
,
oligodactyly
,
osteosclerosis congenita
,
hereditary condition
,
McArdle's disease
,
genetic abnormality
,
hyperbetalipoproteinemia
,
Wilson's disease
,
dystrophy
,
dwarfism
,
congenital afibrinogenemia
,
otosclerosis
,
Fanconi's anaemia
,
juvenile amaurotic idiocy
,
monogenic disorder
,
oligodontia
,
congenital megacolon
,
genetic defect
,
lactase deficiency
,
nevoid elephantiasis
,
mucopolysaccharidosis
,
monogenic disease
,
milk intolerance
,
congenital pancytopenia
,
osteopetrosis
,
Hirschsprung's disease
,
lactose intolerance
,
polygenic disease
,
pachyderma
,
ichthyosis
,
autosomal dominant disease
,
abetalipoproteinemia
,
inborn error of metabolism
,
porphyria
,
disease
,
autosomal recessive disease
,
hereditary disease
,
nanism
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