Methylprednisolone Acetate

Basic Information

Item Value
DrugBank ID DB00959
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 alopecia universalis onychodystrophy vitiligo KG + DL
10 idiopathic steroid-sensitive nephrotic syndrome KG + DL
11 sporadic idiopathic steroid-resistant nephrotic syndrome KG + DL
12 PAGOD syndrome KG + DL
13 disorder of GPI anchor biosynthesis KG + DL
14 persistent polyclonal B-cell lymphocytosis KG + DL
15 46,XY disorder of sex development KG + DL
16 hemoglobinuria KG + DL
17 acquired aplastic anemia KG + DL
18 necrobiosis lipoidica KG + DL
19 articular cartilage disease KG + DL
20 transient arthropathy KG + DL
21 BENTA disease KG + DL
22 severe combined immunodeficiency due to CARD11 deficiency KG + DL
23 de Quervain disease KG + DL
24 ganglion or cyst of synovium/tendon/bursa KG + DL
25 shoulder impingement syndrome KG + DL
26 Behcet syndrome arthropathy KG + DL
27 ankylosis (disease) KG + DL
28 prolapse of lacrimal gland KG + DL
29 adrenomyodystrophy KG + DL
30 spondyloepimetaphyseal dysplasia, Handigodu type KG + DL
31 vertebral joint disease KG + DL
32 alopecia universalis KG + DL
33 platyspondylic dysplasia, Torrance type KG + DL
34 Stickler syndrome KG + DL
35 nephrotic syndrome of childhood - steroid sensitive KG + DL
36 Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome KG + DL
37 autoimmune myocarditis KG + DL
38 megaepiphyseal dwarfism KG + DL
39 Czech dysplasia, metatarsal type KG + DL
40 IMAGe syndrome KG + DL
41 spondylometaphyseal dysplasia, Schmidt type KG + DL
42 subacute bursitis KG + DL
43 Stickler syndrome, type I, nonsyndromic ocular KG + DL
44 anti-glomerular basement membrane disease KG + DL
45 mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis KG + DL
46 spondyloperipheral dysplasia-short ulna syndrome KG + DL
47 pemphigus vegetans KG + DL
48 Sjogren syndrome KG + DL
49 primary hypereosinophilic syndrome KG + DL
50 avascular necrosis of femoral head, primary 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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