Voretigene Neparvovec
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB13932 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 100 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | mitral valve prolapse, myxomatous | KG + DL |
| 2 | pituitary dwarfism | KG + DL |
| 3 | cystic hygroma | KG + DL |
| 4 | conductive hearing loss disorder | KG + DL |
| 5 | susceptibility to mononeuropathy of the median nerve, mild | KG + DL |
| 6 | Wiskott-Aldrich syndrome 2 | KG + DL |
| 7 | non-syndromic esophageal malformation | KG + DL |
| 8 | hypermobility syndrome | KG + DL |
| 9 | woolly hair, autosomal recessive 3 | KG + DL |
| 10 | obsolete hypertension, diastolic, resistance to | KG + DL |
| 11 | obsolete rare tumor of gallbladder and extrahepatic biliary tract | KG + DL |
| 12 | isolated sedoheptulokinase deficiency | KG + DL |
| 13 | ocular tuberculosis | KG + DL |
| 14 | musk, inability to smell | KG + DL |
| 15 | polyhydramnios, chronic idiopathic | KG + DL |
| 16 | cornea plana 1, autosomal dominant | KG + DL |
| 17 | childhood encephalopathy due to thiamine pyrophosphokinase deficiency | KG + DL |
| 18 | hemifacial microsomia | KG + DL |
| 19 | congenital insensitivity to pain-hypohidrosis syndrome | KG + DL |
| 20 | corneal degeneration, band-shaped spheroid | KG + DL |
| 21 | sclerocornea, autosomal dominant | KG + DL |
| 22 | essential fructosuria | KG + DL |
| 23 | enhanced S-cone syndrome | KG + DL |
| 24 | D-glyceric aciduria | KG + DL |
| 25 | sudden cardiac failure, alcohol-induced | KG + DL |
| 26 | congenital hereditary endothelial dystrophy type I | KG + DL |
| 27 | honey-droplet corneal dystrophy | KG + DL |
| 28 | guttate psoriasis | KG + DL |
| 29 | thiopurine S-methyltransferase deficiency | KG + DL |
| 30 | short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | KG + DL |
| 31 | obsolete pathologic fracture | KG + DL |
| 32 | baylisascariasis | KG + DL |
| 33 | Ramon syndrome | KG + DL |
| 34 | congenital hereditary endothelial dystrophy of cornea | KG + DL |
| 35 | IgAD1 | KG + DL |
| 36 | omphalocele (disease) | KG + DL |
| 37 | scleral staphyloma (disease) | KG + DL |
| 38 | cholangiocarcinoma, susceptibility to | KG + DL |
| 39 | hemolytic anemia due to adenylate kinase deficiency | KG + DL |
| 40 | myotonia fluctuans | KG + DL |
| 41 | severe combined immunodeficiency due to CTPS1 deficiency | KG + DL |
| 42 | sunburn | KG + DL |
| 43 | disorder of glutamate decarboxylase | KG + DL |
| 44 | cardiomyopathy associated with myopathy and sudden death | KG + DL |
| 45 | sudden arrhythmia death syndrome | KG + DL |
| 46 | hyperparathyroidism, primary, caused by water clear cell hyperplasia | KG + DL |
| 47 | arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome | KG + DL |
| 48 | Jumping Frenchmen of Maine | KG + DL |
| 49 | pancreas, dorsal, agenesis of | KG + DL |
| 50 | band keratopathy | KG + DL |
(Showing top 50 of 100 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.