Octreotide

Basic Information

Item Value
DrugBank ID DB00104
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 98

Predicted Indications (TxGNN)

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

# Indication Source
1 vulvar inverted follicular keratosis KG + DL
2 seborrheic keratosis KG + DL
3 nephrotic syndrome ocular anomalies KG + DL
4 Addison disease KG + DL
5 membranoproliferative glomerulonephritis, X-linked KG + DL
6 familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis KG + DL
7 familial idiopathic steroid-resistant nephrotic syndrome with minimal changes KG + DL
8 adrenocortical insufficiency KG + DL
9 primary hypereosinophilic syndrome KG + DL
10 autosomal recessive familial Mediterranean fever KG + DL
11 primary hereditary glaucoma KG + DL
12 secondary hypereosinophilic syndrome KG + DL
13 familial nephrotic syndrome KG + DL
14 open-angle glaucoma KG + DL
15 familial Mediterranean fever, autosomal dominant KG + DL
16 retinal telangiectasia KG + DL
17 renal-hepatic-pancreatic dysplasia KG + DL
18 Smouldering systemic mastocytosis KG + DL
19 gout KG + DL
20 lymphoadenopathic mastocytosis with eosinophilia KG + DL
21 dermatofibrosarcoma protuberans KG + DL
22 arteriosclerotic retinopathy KG + DL
23 retinal microaneurysm KG + DL
24 46,XY disorder of sex development KG + DL
25 vertebral artery occlusion KG + DL
26 retinal artery occlusion KG + DL
27 karyomegalic interstitial nephritis KG + DL
28 humoral hypercalcemia of malignancy KG + DL
29 Joubert syndrome with renal defect KG + DL
30 polycystic kidney disease 3 with or without polycystic liver disease KG + DL
31 eosinophilic pneumonia KG + DL
32 thoracic malformation KG + DL
33 chronic tic disorder KG + DL
34 systemic mastocytosis KG + DL
35 steroid-resistant nephrotic syndrome KG + DL
36 psychogenic movement disorders KG + DL
37 benign shuddering attacks KG + DL
38 extrapyramidal and movement disease KG + DL
39 adult familial nephronophthisis-spastic quadriparesia syndrome KG + DL
40 Plasmodium falciparum malaria KG + DL
41 primary orthostatic tremor KG + DL
42 glaucoma 1, open angle KG + DL
43 benign paroxysmal tonic upgaze of childhood with ataxia KG + DL
44 tremor-nystagmus-duodenal ulcer syndrome KG + DL
45 inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency KG + DL
46 Pierson syndrome KG + DL
47 Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency KG + DL
48 subarachnoid hemorrhage (disease) KG + DL
49 fibroma of prostate KG + DL
50 adrenomyodystrophy KG + DL

(Showing top 50 of 98 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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