Yohimbine Hydrochloride

Basic Information

Item Value
DrugBank ID DB01392
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 attention deficit-hyperactivity disorder KG + DL
4 faciodigitogenital syndrome KG + DL
5 migraine with or without aura, susceptibility to KG + DL
6 primary hereditary glaucoma KG + DL
7 headache disorder KG + DL
8 transient ischemic attack (disease) KG + DL
9 common cold KG + DL
10 open-angle glaucoma KG + DL
11 atrophoderma vermiculata KG + DL
12 trigeminal autonomic cephalalgia KG + DL
13 pulmonary hypertension KG + DL
14 ulerythema ophryogenesis KG + DL
15 papillary conjunctivitis KG + DL
16 kyphoscoliotic heart disease KG + DL
17 allergic urticaria KG + DL
18 respiratory failure KG + DL
19 attention deficit hyperactivity disorder, inattentive type KG + DL
20 trichotillomania KG + DL
21 erectile dysfunction (disease) KG + DL
22 chondromyxoid fibroma KG + DL
23 cold urticaria KG + DL
24 Tourette syndrome KG + DL
25 specific developmental disorder KG + DL
26 glaucoma 1, open angle KG + DL
27 phaeochromocytoma KG + DL
28 pulmonary hypertension, primary, autosomal recessive KG + DL
29 nephrogenic syndrome of inappropriate antidiuresis KG + DL
30 nasal cavity disease KG + DL
31 cor pulmonale KG + DL
32 intracranial arteriosclerosis KG + DL
33 congenital hypotrichosis milia KG + DL
34 hypotrichosis simplex of the scalp KG + DL
35 venous thoracic outlet syndrome KG + DL
36 arterial thoracic outlet syndrome KG + DL
37 neurogenic thoracic outlet syndrome KG + DL
38 vascular disease KG + DL
39 diffuse alopecia areata KG + DL
40 exercise-induced malignant hyperthermia KG + DL
41 sciatic neuropathy KG + DL
42 obsolete patella aplasia, coxa vara, and tarsal synostosis KG + DL
43 psychotic disorder KG + DL
44 visceral calciphylaxis KG + DL
45 familial periodic paralysis KG + DL
46 subarachnoid hemorrhage (disease) KG + DL
47 bronchial disease KG + DL
48 idiopathic and/or familial pulmonary arterial hypertension KG + DL
49 open angle glaucoma 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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