Betamethasone Dipropionate

Basic Information

Item Value
DrugBank ID DB00443
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 alopecia areata KG + DL
2 alopecia mucinosa KG + DL
3 telogen effluvium KG + DL
4 Quinquaud’s folliculitis decalvans KG + DL
5 alopecia antibody deficiency KG + DL
6 hereditary hypotrichosis with recurrent skin vesicles KG + DL
7 alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome KG + DL
8 atrichia with papular lesions KG + DL
9 idiopathic steroid-sensitive nephrotic syndrome KG + DL
10 sporadic idiopathic steroid-resistant nephrotic syndrome KG + DL
11 alopecia universalis onychodystrophy vitiligo KG + DL
12 necrobiosis lipoidica KG + DL
13 autoimmune myocarditis KG + DL
14 disorder of GPI anchor biosynthesis KG + DL
15 46,XY disorder of sex development KG + DL
16 Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome KG + DL
17 PAGOD syndrome KG + DL
18 acquired aplastic anemia KG + DL
19 hemoglobinuria KG + DL
20 disease of orbital part of eye adnexa KG + DL
21 nephrotic syndrome ocular anomalies KG + DL
22 cystic teratoma KG + DL
23 spinal cord dermoid cyst KG + DL
24 dermoid cyst of ovary KG + DL
25 subacute bursitis KG + DL
26 persistent polyclonal B-cell lymphocytosis KG + DL
27 punctate epithelial keratoconjunctivitis KG + DL
28 nephrotic syndrome of childhood - steroid sensitive KG + DL
29 articular cartilage disease KG + DL
30 transient arthropathy KG + DL
31 shoulder impingement syndrome KG + DL
32 ganglion or cyst of synovium/tendon/bursa KG + DL
33 Behcet syndrome arthropathy KG + DL
34 de Quervain disease KG + DL
35 membranoproliferative glomerulonephritis, X-linked KG + DL
36 adrenomyodystrophy KG + DL
37 ankylosis (disease) KG + DL
38 vulvar inverted follicular keratosis KG + DL
39 prolapse of lacrimal gland KG + DL
40 BENTA disease KG + DL
41 severe combined immunodeficiency due to CARD11 deficiency KG + DL
42 familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis KG + DL
43 familial idiopathic steroid-resistant nephrotic syndrome with minimal changes KG + DL
44 congenital nephrotic syndrome, Finnish type KG + DL
45 vertebral joint disease KG + DL
46 alopecia universalis KG + DL
47 lacrimal gland neoplasm KG + DL
48 lens subluxation (disease) KG + DL
49 aphthous stomatitis KG + DL
50 IMAGe syndrome 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.


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