Isocarboxazid

Basic Information

Item Value
DrugBank ID DB01247
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 51

Predicted Indications (TxGNN)

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

# Indication Source
1 benign paroxysmal torticollis of infancy KG + DL
2 agoraphobia KG + DL
3 obsessive-compulsive disorder KG + DL
4 neurotic disorder KG + DL
5 phobic disorder KG + DL
6 post-traumatic stress disorder KG + DL
7 dysthymic disorder KG + DL
8 melancholia KG + DL
9 neurotic depression KG + DL
10 schizoid personality disorder KG + DL
11 paranoid personality disorder KG + DL
12 histrionic personality disorder (disease) KG + DL
13 schizotypal personality disorder KG + DL
14 Ohdo syndrome and variants KG + DL
15 blepharophimosis - intellectual disability syndrome, Ohdo type KG + DL
16 Keppen-Lubinsky syndrome KG + DL
17 ligneous conjunctivitis KG + DL
18 autosomal dominant slowed nerve conduction velocity KG + DL
19 congenital isolated adrenocorticotropic hormone deficiency (disease) KG + DL
20 mixed anxiety and depressive disorder KG + DL
21 childhood apraxia of speech KG + DL
22 dependent personality disorder KG + DL
23 vitamin B12-responsive methylmalonic acidemia KG + DL
24 surfactant metabolism dysfunction, pulmonary KG + DL
25 narcissistic personality disorder KG + DL
26 chromosome 15q26-qter deletion syndrome KG + DL
27 avoidant personality disorder KG + DL
28 postpartum depression KG + DL
29 coronary aneurysm KG + DL
30 Asperger syndrome KG + DL
31 familial hypertryptophanemia KG + DL
32 chondromyxoid fibroma KG + DL
33 attention deficit hyperactivity disorder, inattentive type KG + DL
34 manic bipolar affective disorder KG + DL
35 chromosome 2P16.3 deletion syndrome KG + DL
36 distal 17p13.3 microdeletion syndrome KG + DL
37 myofascial pain syndrome KG + DL
38 Pitt-Hopkins-like syndrome 2 KG + DL
39 specific developmental disorder KG + DL
40 syndromic myopia KG + DL
41 polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis KG + DL
42 phyllodes tumor KG + DL
43 nicotine dependence KG + DL
44 myopia X-linked KG + DL
45 Charcot-Marie-Tooth disease, demyelinating, type 1G KG + DL
46 retinal dystrophy with or without extraocular anomalies KG + DL
47 osteoarthritis susceptibility KG + DL
48 congenital disorder of glycosylation with defective fucosylation KG + DL
49 hydranencephaly (disease) KG + DL
50 attention deficit-hyperactivity disorder KG + DL

(Showing top 50 of 51 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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