Identifier (URI) | Rank |
---|---|
isac:inheritable_disease_ | 5.88129e-14 |
dbr:Genetic_disorder | 5.88129e-14 |
isac:polygenic_disorder_ | 5.88129e-14 |
isac:single-gene_disorder_ | 5.88129e-14 |
isac:monogenic_disorder_ | 5.88129e-14 |
isac:x-linked+genetic_disorder_ | 5.88129e-14 |
isac:human+genetic_disease_ | 5.88129e-14 |
isac:heritable_disease_ | 5.88129e-14 |
isac:genetic_defect_ | 5.88129e-14 |
isac:hereditary_disease_ | 5.88129e-14 |
isac:genetic_disorder_ | 5.88129e-14 |
isac:genetic_condition_ | 5.88129e-14 |
isac:genetic_disease_ | 5.88129e-14 |
isac:complex_disease_ | 5.88129e-14 |
isac:hereditary_condition_ | 5.88129e-14 |
isac:genetic_illness_ | 5.88129e-14 |
isac:monogenic_disease_ | 5.88129e-14 |
isac:mendelian_disease_ | 5.88129e-14 |
isac:single+gene_disorder_ | 5.88129e-14 |
isac:genetic_anomaly_ | 5.88129e-14 |