Dexmedetomidine

Basic Information

Item Value
DrugBank ID DB00633
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 nephrogenic syndrome of inappropriate antidiuresis KG + DL
2 migraine disorder KG + DL
3 migraine with brainstem aura KG + DL
4 headache disorder KG + DL
5 trigeminal autonomic cephalalgia KG + DL
6 pulmonary hypertension KG + DL
7 hypotrichosis simplex of the scalp KG + DL
8 migraine with or without aura, susceptibility to KG + DL
9 atrophoderma vermiculata KG + DL
10 congenital hypotrichosis milia KG + DL
11 diffuse alopecia areata KG + DL
12 ulerythema ophryogenesis KG + DL
13 alopecia KG + DL
14 kyphoscoliotic heart disease KG + DL
15 Tourette syndrome KG + DL
16 open-angle glaucoma KG + DL
17 primary hereditary glaucoma KG + DL
18 bronchial disease KG + DL
19 trichotillomania KG + DL
20 tendinitis KG + DL
21 myositis fibrosa KG + DL
22 idiopathic granulomatous myositis KG + DL
23 fibromyalgia KG + DL
24 dysthymic disorder KG + DL
25 common cold KG + DL
26 nephrogenic diabetes insipidus KG + DL
27 subarachnoid hemorrhage (disease) KG + DL
28 endobronchial leiomyoma KG + DL
29 endobronchial lipoma KG + DL
30 bronchus adenoma KG + DL
31 inclusion body myositis KG + DL
32 hypertrichosis (disease) KG + DL
33 pulmonary hypertension, primary, autosomal recessive KG + DL
34 malformation syndrome with odontal and/or periodontal component KG + DL
35 syndrome with a Dandy-Walker malformation as major feature KG + DL
36 Ambras type hypertrichosis universalis congenita KG + DL
37 small intestine cancer KG + DL
38 obsolete patella aplasia, coxa vara, and tarsal synostosis KG + DL
39 isolated genetic hair shaft abnormality KG + DL
40 diabetes insipidus, nephrogenic, X-linked KG + DL
41 congestive heart failure KG + DL
42 acute pulmonary heart disease KG + DL
43 cough variant asthma KG + DL
44 idiopathic and/or familial pulmonary arterial hypertension KG + DL
45 paratenonitis KG + DL
46 duodenum cancer KG + DL
47 calcific tendinitis KG + DL
48 genetic alopecia KG + DL
49 pulmonary arterial hypertension KG + DL
50 chromosome 17q23.1-q23.2 deletion 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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