en
oligodontia
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
autosomal recessive disease
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
maple syrup urine disease
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
monogenic disorder
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
muscular dystrophy
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
lactose intolerance
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
osteopetrosis
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
genetic disease
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
otosclerosis
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
mucopolysaccharidosis
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
Hirschsprung's disease
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
McArdle's disease
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
Spielmeyer-Vogt disease
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
ichthyosis
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
nevoid elephantiasis
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
hyperbetalipoproteinemia
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
abetalipoproteinemia
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
congenital afibrinogenemia
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
hepatolenticular degeneration
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
dwarfism
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
autosomal dominant disease
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
oligodactyly
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
polygenic disorder
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
inborn error of metabolism
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
Fanconi's anemia
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
achondroplasia
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|
en
porphyria
(n, state)
|
― IsA ⟶
Weight: 2.0
|
en
genetic disease
(n, state)
|
Source: Open Multilingual WordNet
|