Haloperidol

Basic Information

Item Value
DrugBank ID DB00502
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 39

Predicted Indications (TxGNN)

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

# Indication Source
1 congenital disorder of glycosylation with defective fucosylation KG + DL
2 retinal dystrophy with or without extraocular anomalies KG + DL
3 hydranencephaly (disease) KG + DL
4 myopia X-linked KG + DL
5 Charcot-Marie-Tooth disease, demyelinating, type 1G KG + DL
6 myopia 26, X-linked, female-limited KG + DL
7 syndromic myopia KG + DL
8 polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis KG + DL
9 atypical glycine encephalopathy KG + DL
10 manic bipolar affective disorder KG + DL
11 early-onset schizophrenia KG + DL
12 treatment-refractory schizophrenia KG + DL
13 trichotillomania KG + DL
14 REM sleep behavior disorder KG + DL
15 psychosexual disorder KG + DL
16 attention deficit-hyperactivity disorder KG + DL
17 skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome KG + DL
18 neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive KG + DL
19 postpartum psychosis KG + DL
20 substance-induced psychosis KG + DL
21 faciodigitogenital syndrome KG + DL
22 enuresis KG + DL
23 factitious disorder KG + DL
24 dissociative disorder KG + DL
25 distal 17p13.3 microdeletion syndrome KG + DL
26 attention deficit hyperactivity disorder, inattentive type KG + DL
27 hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome KG + DL
28 major affective disorder KG + DL
29 bipolar disorder KG + DL
30 chondromyxoid fibroma KG + DL
31 specific developmental disorder KG + DL
32 drug/alcohol-induced mental disorder KG + DL
33 alcoholic psychosis KG + DL
34 Malan overgrowth syndrome KG + DL
35 tic disorder KG + DL
36 diabetes insipidus, nephrogenic, autosomal KG + DL
37 partial deletion of the short arm of chromosome 4 KG + DL
38 cognitive disorder KG + DL
39 impulse control disorder KG + DL

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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