Fosnetupitant
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB14019 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 42 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | leprosy | KG + DL |
| 2 | mycotic corneal ulcer | KG + DL |
| 3 | coronary artery disease | KG + DL |
| 4 | anomalous left coronary artery from the pulmonary artery | KG + DL |
| 5 | candidiasis | KG + DL |
| 6 | myocardial ischemia | KG + DL |
| 7 | uterine polyp | KG + DL |
| 8 | polyp of vocal cord | KG + DL |
| 9 | polyp of middle ear | KG + DL |
| 10 | polyp of ureter | KG + DL |
| 11 | polyp of frontal sinus | KG + DL |
| 12 | epulis | KG + DL |
| 13 | polyp of external auditory canal | KG + DL |
| 14 | fibroepithelial polyp | KG + DL |
| 15 | polyp of vulva | KG + DL |
| 16 | neoplastic polyp | KG + DL |
| 17 | hypertrichosis (disease) | KG + DL |
| 18 | hyperargininemia | KG + DL |
| 19 | malformation syndrome with odontal and/or periodontal component | KG + DL |
| 20 | Ambras type hypertrichosis universalis congenita | KG + DL |
| 21 | oral candidiasis | KG + DL |
| 22 | syndrome with a Dandy-Walker malformation as major feature | KG + DL |
| 23 | isolated genetic hair shaft abnormality | KG + DL |
| 24 | osteoradionecrosis of the mandible | KG + DL |
| 25 | commissural lip fistula | KG + DL |
| 26 | burning mouth syndrome | KG + DL |
| 27 | oral leukoedema | KG + DL |
| 28 | genetic multiple congenital anomalies/dysmorphic syndrome without intellectual disability | KG + DL |
| 29 | Laubry-Pezzi syndrome | KG + DL |
| 30 | heart disease | KG + DL |
| 31 | interventricular septum aneurysm | KG + DL |
| 32 | genetic syndromic Pierre Robin syndrome | KG + DL |
| 33 | Pierre Robin syndrome associated with a chromosomal anomaly | KG + DL |
| 34 | Jeune syndrome situs inversus | KG + DL |
| 35 | disorder of fucoglycosan synthesis | KG + DL |
| 36 | orofacial clefting syndrome | KG + DL |
| 37 | partial deletion of the long arm of chromosome 7 | KG + DL |
| 38 | amenorrhea (disease) | KG + DL |
| 39 | kyphoscoliotic heart disease | KG + DL |
| 40 | partial deletion of the long arm of chromosome 22 | KG + DL |
| 41 | pulmonary hypertension | KG + DL |
| 42 | pulmonary valve disease | KG + DL |
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.