Procyclidine Hcl

Basic Information

Item Value
DrugBank ID DB00387
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 73

Predicted Indications (TxGNN)

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

# Indication Source
1 Rasmussen subacute encephalitis KG + DL
2 myelitis KG + DL
3 PLA2G6-associated neurodegeneration KG + DL
4 attention deficit-hyperactivity disorder KG + DL
5 faciodigitogenital syndrome KG + DL
6 transaldolase deficiency KG + DL
7 progressive supranuclear palsy-corticobasal syndrome KG + DL
8 paralysis agitans, juvenile, of Hunt KG + DL
9 polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis KG + DL
10 fructose-1,6-bisphosphatase deficiency KG + DL
11 congenital disorder of glycosylation with defective fucosylation KG + DL
12 retinal dystrophy with or without extraocular anomalies KG + DL
13 Charcot-Marie-Tooth disease, demyelinating, type 1G KG + DL
14 Lewy body dementia KG + DL
15 atypical glycine encephalopathy KG + DL
16 myopia 26, X-linked, female-limited KG + DL
17 X-linked intellectual disability-ataxia-apraxia syndrome KG + DL
18 myopia X-linked KG + DL
19 X-linked intellectual disability-cerebellar hypoplasia syndrome KG + DL
20 lethal infantile mitochondrial myopathy KG + DL
21 CLCN4-related X-linked intellectual disability syndrome KG + DL
22 X-linked intellectual disability-spastic quadriparesis syndrome KG + DL
23 X-linked spasticity-intellectual disability-epilepsy syndrome KG + DL
24 attention deficit hyperactivity disorder, inattentive type KG + DL
25 syndromic myopia KG + DL
26 hydrocephaly-cerebellar agenesis syndrome KG + DL
27 X-linked intellectual disability with hypopituitarism KG + DL
28 syndromic X-linked intellectual disability Chudley-Schwartz type KG + DL
29 intellectual disability, X-linked, syndromic KG + DL
30 X-linked cerebral-cerebellar-coloboma syndrome syndrome KG + DL
31 Paganini-Miozzo syndrome KG + DL
32 X-linked intellectual disability-hypotonia-movement disorder syndrome KG + DL
33 Prieto syndrome KG + DL
34 X-linked intellectual disability, Stocco dos Santos type KG + DL
35 intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type KG + DL
36 hydranencephaly (disease) KG + DL
37 Basilicata-Akhtar syndrome KG + DL
38 NAA10-related syndrome KG + DL
39 X-linked intellectual disability-craniofacioskeletal syndrome KG + DL
40 MED12-related intellectual disability syndrome KG + DL
41 X-linked intellectual disability-precocious puberty-obesity syndrome KG + DL
42 schizophrenia KG + DL
43 holoprosencephaly 13, X-linked KG + DL
44 lissencephaly type 1 due to doublecortin gene mutation KG + DL
45 X-linked intellectual disability-acromegaly-hyperactivity syndrome KG + DL
46 autosomal recessive Parkinson disease KG + DL
47 specific developmental disorder KG + DL
48 dystonia KG + DL
49 dystonia, focal, task-specific KG + DL
50 multiple system atrophy, parkinsonian type KG + DL

(Showing top 50 of 73 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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