Sulfadiazine

Basic Information

Item Value
DrugBank ID DB00359
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 66

Predicted Indications (TxGNN)

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

# Indication Source
1 pneumocystosis KG + DL
2 punctate epithelial keratoconjunctivitis KG + DL
3 dermatitis herpetiformis KG + DL
4 exposure keratitis KG + DL
5 acne (disease) KG + DL
6 vestibular neuronitis KG + DL
7 brachial plexus neuritis KG + DL
8 seborrheic keratosis KG + DL
9 rheumatoid arthritis KG + DL
10 non-human animal disease KG + DL
11 motor nerve neuritis KG + DL
12 vulvar inverted follicular keratosis KG + DL
13 vernal keratoconjunctivitis KG + DL
14 leprosy KG + DL
15 neurotrophic keratopathy KG + DL
16 brachydactyly-syndactyly syndrome KG + DL
17 nocardiosis KG + DL
18 ulcerative proctosigmoiditis KG + DL
19 colobomatous microphthalmia-rhizomelic dysplasia syndrome KG + DL
20 familial acanthosis nigricans KG + DL
21 osteoarthritis susceptibility KG + DL
22 epidemic keratoconjunctivitis KG + DL
23 urticaria, familial localized heat KG + DL
24 furuncular myiasis KG + DL
25 wound myiasis KG + DL
26 creeping myiasis KG + DL
27 ocular toxoplasmosis KG + DL
28 aplasia cutis-myopia syndrome KG + DL
29 osteoarthritis KG + DL
30 Tietz syndrome KG + DL
31 van den Bosch syndrome KG + DL
32 cutaneous photosensitivity-lethal colitis syndrome KG + DL
33 acquired thrombocytopenia KG + DL
34 inherited cutis laxa KG + DL
35 cap polyposis KG + DL
36 neonatal inflammatory skin and bowel disease KG + DL
37 X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome KG + DL
38 heparin-induced thrombocytopenia (disease) KG + DL
39 familial pityriasis rubra pilaris KG + DL
40 endocardial fibroelastosis KG + DL
41 pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa KG + DL
42 erythrokeratodermia-cardiomyopathy syndrome KG + DL
43 urticaria, aquagenic KG + DL
44 nail infection KG + DL
45 acromesomelic dysplasia, Hunter-Thompson type KG + DL
46 keratosis follicularis-dwarfism-cerebral atrophy syndrome KG + DL
47 anhidrosis, familial generalized, with abnormal or absent sweat glands KG + DL
48 congenital hypotrichosis with juvenile macular dystrophy KG + DL
49 familial primary localized cutaneous amyloidosis KG + DL
50 undetermined colitis KG + DL

(Showing top 50 of 66 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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