Osilodrostat

Basic Information

Item Value
DrugBank ID DB11837
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 90

Predicted Indications (TxGNN)

The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.

# Indication Source
1 familial generalized lentiginosis KG + DL
2 congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome KG + DL
3 acromelanosis KG + DL
4 gastrocutaneous syndrome KG + DL
5 leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome KG + DL
6 Moynahan syndrome KG + DL
7 rhabdoid tumor KG + DL
8 X-linked lymphoproliferative disease due to SH2D1A deficiency KG + DL
9 osteopathia striata-pigmentary dermopathy-white forelock syndrome KG + DL
10 peripheral nerve schwannoma KG + DL
11 schwannoma of twelfth cranial nerve KG + DL
12 sympathetic neurilemmoma KG + DL
13 microcystic/reticular schwannoma KG + DL
14 trigeminal schwannoma KG + DL
15 A20 haploinsufficiency KG + DL
16 benign neoplasm of adrenal gland KG + DL
17 immune dysregulation with inflammatory bowel disease KG + DL
18 Steel syndrome KG + DL
19 hemophagocytic syndrome associated with an infection KG + DL
20 acquired hemophagocytic lymphohistiocytosis associated with malignant disease KG + DL
21 autosomal recessive familial Mediterranean fever KG + DL
22 autosomal ichthyosis syndrome with fatal disease course KG + DL
23 mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies KG + DL
24 proximal myopathy with extrapyramidal signs KG + DL
25 hypophosphatasia KG + DL
26 Gaucher disease KG + DL
27 skeletal muscle disease KG + DL
28 familial apolipoprotein C-II deficiency KG + DL
29 polycystic kidney disease 3 with or without polycystic liver disease KG + DL
30 familial Mediterranean fever, autosomal dominant KG + DL
31 autosomal dominant keratitis KG + DL
32 primary immunodeficiency due to a genetic defect in innate immunity KG + DL
33 familial Mediterranean fever KG + DL
34 inclusion myopathy KG + DL
35 autosomal dominant Alport syndrome KG + DL
36 lipoatrophic diabetes KG + DL
37 neurofibromatosis KG + DL
38 renal-hepatic-pancreatic dysplasia KG + DL
39 hemophagocytic lymphohistiocytosis KG + DL
40 autosomal dominant brachyolmia KG + DL
41 extracutaneous mastocytoma KG + DL
42 lipodystrophy-intellectual disability-deafness syndrome KG + DL
43 citrullinemia, type II, adult-onset KG + DL
44 arthrogryposis, distal, KG + DL
45 X-linked lymphoproliferative syndrome KG + DL
46 TSH producing pituitary tumor KG + DL
47 thoracic malformation KG + DL
48 lipodystrophy due to peptidic growth factors deficiency KG + DL
49 autosomal dominant complex spastic paraplegia KG + DL
50 autosomal dominant pure spastic paraplegia KG + DL

(Showing top 50 of 90 predictions)

Disclaimer

These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.


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