Camphor

Basic Information

Item Value
DrugBank ID DB01744
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 migraine disorder KG + DL
2 migraine with brainstem aura KG + DL
3 erectile dysfunction (disease) KG + DL
4 pulmonary hypertension KG + DL
5 migraine with or without aura, susceptibility to KG + DL
6 kyphoscoliotic heart disease KG + DL
7 ulerythema ophryogenesis KG + DL
8 Raynaud disease KG + DL
9 atrophoderma vermiculata KG + DL
10 Tourette syndrome KG + DL
11 atypical coarctation of aorta KG + DL
12 intermittent vascular claudication KG + DL
13 peripheral vascular disease KG + DL
14 trichotillomania KG + DL
15 intracranial arteriosclerosis KG + DL
16 adrenal gland hyperfunction KG + DL
17 multiple endocrine neoplasia KG + DL
18 peripheral arterial disease KG + DL
19 Monckeberg arteriosclerosis KG + DL
20 His bundle tachycardia KG + DL
21 sciatic neuropathy KG + DL
22 multifocal atrial tachycardia (disease) KG + DL
23 localized pagetoid reticulosis KG + DL
24 lichen disease KG + DL
25 Prinzmetal angina KG + DL
26 aortic malformation KG + DL
27 postural orthostatic tachycardia syndrome KG + DL
28 ventricular tachycardia KG + DL
29 cauda equina syndrome KG + DL
30 acute lymphoblastic leukemia (disease) KG + DL
31 idiopathic neonatal atrial flutter KG + DL
32 congenital adrenal hyperplasia KG + DL
33 Treacher-Collins syndrome 1 KG + DL
34 endemic goiter KG + DL
35 acrofacial dysostosis, Palagonia type KG + DL
36 lesion of sciatic nerve KG + DL
37 obsolete bundle branch block KG + DL
38 Nager acrofacial dysostosis KG + DL
39 keratosis pilaris KG + DL
40 pulmonary hypertension, primary, autosomal recessive KG + DL
41 acrofacial dysostosis KG + DL
42 lichen planus pigmentosus KG + DL
43 annular atrophic lichen planus KG + DL
44 hypertrophic lichen planus KG + DL
45 lichen planus pemphigoides KG + DL
46 catecholaminergic polymorphic ventricular tachycardia KG + DL
47 absence epilepsy KG + DL
48 Graves disease KG + DL
49 chromosome 17q23.1-q23.2 deletion syndrome KG + DL
50 primary cutaneous T-cell lymphoma 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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