Methysergide

Basic Information

Item Value
DrugBank ID DB00247
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 96

Predicted Indications (TxGNN)

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

# Indication Source
1 migraine disorder KG + DL
2 migraine with brainstem aura KG + DL
3 migraine with or without aura, susceptibility to KG + DL
4 atrophoderma vermiculata KG + DL
5 ulerythema ophryogenesis KG + DL
6 pulmonary hypertension KG + DL
7 kyphoscoliotic heart disease KG + DL
8 dysthymic disorder KG + DL
9 hypertrichosis (disease) KG + DL
10 amenorrhea (disease) KG + DL
11 Ambras type hypertrichosis universalis congenita KG + DL
12 sciatic neuropathy KG + DL
13 malformation syndrome with odontal and/or periodontal component KG + DL
14 syndrome with a Dandy-Walker malformation as major feature KG + DL
15 isolated genetic hair shaft abnormality KG + DL
16 obsolete patella aplasia, coxa vara, and tarsal synostosis KG + DL
17 tendinitis KG + DL
18 pulmonary hypertension, primary, autosomal recessive KG + DL
19 erectile dysfunction (disease) KG + DL
20 coxopodopatellar syndrome KG + DL
21 fibromyalgia KG + DL
22 familial clubfoot due to 17q23.1q23.2 microduplication KG + DL
23 myositis fibrosa KG + DL
24 idiopathic granulomatous myositis KG + DL
25 chromosome 17q23.1-q23.2 deletion syndrome KG + DL
26 idiopathic pulmonary arterial hypertension KG + DL
27 Tourette syndrome KG + DL
28 pulmonary hypertension, primary KG + DL
29 headache disorder KG + DL
30 inclusion body myositis KG + DL
31 neurotic disorder KG + DL
32 idiopathic and/or familial pulmonary arterial hypertension KG + DL
33 mycotic corneal ulcer KG + DL
34 peripheral arterial disease KG + DL
35 gastrointestinal hamartoma KG + DL
36 trichotillomania KG + DL
37 endogenous depression KG + DL
38 Ohdo syndrome and variants KG + DL
39 benign prostatic hyperplasia (disease) KG + DL
40 Prinzmetal angina KG + DL
41 neuroblastoma KG + DL
42 peripheral vascular disease KG + DL
43 heritable pulmonary arterial hypertension KG + DL
44 intermittent vascular claudication KG + DL
45 trigeminal autonomic cephalalgia KG + DL
46 neurotic depression KG + DL
47 melancholia KG + DL
48 vertebral anomalies and variable endocrine and T-cell dysfunction KG + DL
49 congenital isolated adrenocorticotropic hormone deficiency (disease) KG + DL
50 pulmonary arterial hypertension KG + DL

(Showing top 50 of 96 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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