Genetic: Non invasive prenatal diagnosis
( DrugBank: - / KEGG DRUG: - )
3 diseases
8. ハンチントン病
臨床試験数 : 296 / 薬物数 : 245 - (DrugBank : 63) / 標的遺伝子数 : 89 - 標的パスウェイ数 : 165
| No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
|---|
113. 筋ジストロフィー
臨床試験数 : 826 / 薬物数 : 680 - (DrugBank : 126) / 標的遺伝子数 : 86 - 標的パスウェイ数 : 188
| No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
|---|
206. 脆弱Ｘ症候群
臨床試験数 : 124 / 薬物数 : 103 - (DrugBank : 35) / 標的遺伝子数 : 58 - 標的パスウェイ数 : 84
| No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
|---|