Disease 指定難病
疾患数 : 348 - 臨床試験総数 : 43,690 / 薬物総数 : 27,527 - ( DrugBank : 2,441 ) / 標的遺伝子総数 : 714 - 標的パスウェイ総数 : 315
| 告示 番号 | 疾患名 [疾患群] | 臨床試験数 | Phase 1 / 2 / 3 / 4 | 薬物数 [ DrugBank ] | 標的遺伝子数 | パスウェイ数 | 国内患者数 R6年度医療費受給者証所持者数(修正版) |
|---|---|---|---|---|---|
| 90 | 網膜色素変性症 [視] 💬 "Retinitis pigmentosa", "Rod dystrophy", "Cone-rod dystrophy", "Rod-Cone Dystrophy" | 203 203 trials | 83 / 105 / 52 / 0 💬 | 267 267 drugs [ 49 49 drugs ] | 55 55 genes | 162 pathways | 19991 19,991人年齢分布
|
| 134 | 中隔視神経形成異常症/ドモルシア症候群 [視] 💬 "Septo-optic dysplasia", "De Morsier syndrome" | 3 3 trials | 0 / 0 / 1 / 0 💬 | 3 3 drugs [ 1 1 drug ] | 1 1 gene | 3 pathways | 16 16人年齢分布
|
| 164 | 眼皮膚白皮症 [視] 💬 "Oculocutaneous albinism", "Hermansky-Pudlak syndrome", "HPS", "Chediak-Higashi syndrome", "Chédiak-Higashi syndrome", "CHS", "Griscelli syndrome" | 17 17 trials | 2 / 7 / 1 / 0 💬 | 57 57 drugs [ 32 32 drugs ] | 32 32 genes | 139 pathways | 32 32人年齢分布
|
| 301 | 黄斑ジストロフィー [視] 💬 "Macular dystrophy", "Vitelliform macular dystrophy", "Best vitelliform macular dystrophy", "Best disease", "Stargardt disease", "Occult macular dystrophy", "Cone dystrophy", "Cone rod dystrophy", "X-linked juvenile retinoschisis", "Central areolar choroidal dystrophy" | 69 69 trials | 22 / 34 / 14 / 0 💬 | 66 66 drugs [ 15 15 drugs ] | 10 10 genes | 80 pathways | 262 262人年齢分布
|
| 302 | レーベル遺伝性視神経症 [視] 💬 "Leber hereditary optic neuropathy", "LHON", "Leber hereditary optic atrophy", "Leber disease" | 47 47 trials | 6 / 11 / 19 / 10 💬 | 36 36 drugs [ 8 8 drugs ] | 5 5 genes | 33 pathways | 134 134人年齢分布
|
| 303 | アッシャー症候群 [聴] 💬 [視] 💬 "Usher syndrome" | 16 16 trials | 1 / 2 / 0 / 0 💬 | 27 27 drugs [ 6 6 drugs ] | 1 1 gene | 1 pathway | 30 30人年齢分布
|
| 328 | 前眼部形成異常 [視] 💬 "Anterior segment dysgenesis", "ASD" | 0 - | 0 - | 0 - | 21 21人年齢分布
|
| 329 | 無虹彩症 [視] 💬 "Aniridia" | 5 5 trials | 0 / 2 / 0 / 0 💬 | 6 6 drugs [ 2 2 drugs ] | 0 - | 157 157人年齢分布
|
| 332 | 膠様滴状角膜ジストロフィー [視] 💬 "Gelatinous drop-like corneal dystrophy" | 0 - | 0 - | 0 - | 9 9人年齢分布
|
