ConceptNet 5: Query results

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