Dornase Alfa

Basic Information

Item Value
DrugBank ID DB00003
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 pyridoxine-dependent epilepsy caused by ALDH7A1 mutant KG + DL
2 hereditary glaucoma KG + DL
3 vaginal villous adenoma KG + DL
4 osteoclastic giant cell tumor of pancreas KG + DL
5 anaerobic cellulitis KG + DL
6 glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form KG + DL
7 granulomatous hypophysitis KG + DL
8 disease by cellular process disrupted KG + DL
9 intermediate severe Salla disease KG + DL
10 mesothelial neoplasm KG + DL
11 melanocytic skin neoplasm KG + DL
12 lymphoid hemopathy KG + DL
13 steroid-induced glaucoma KG + DL
14 lipomatous cancer KG + DL
15 genetic infertility KG + DL
16 bone marrow neoplasm KG + DL
17 clear cell sarcoma KG + DL
18 smooth muscle cancer KG + DL
19 non-small cell squamous lung carcinoma KG + DL
20 Epstein-Barr virus-associated mesenchymal tumor KG + DL
21 generalized galactose epimerase deficiency KG + DL
22 human herpesvirus 8-related tumor KG + DL
23 Orthocoronavirinae infectious disease KG + DL
24 human herpesvirus 8 infection KG + DL
25 inner ear cancer KG + DL
26 deafness, autosomal recessive KG + DL
27 glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form KG + DL
28 congenital stationary night blindness autosomal dominant KG + DL
29 Pseudomonas aeruginosa infectious disease KG + DL
30 osteogenesis imperfecta KG + DL
31 iodine hypothyroidism KG + DL
32 ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies KG + DL
33 CNS demyelinating autoimmune disease KG + DL
34 craniosynostosis-intracranial calcifications syndrome KG + DL
35 indolent B-cell non-Hodgkin lymphoma KG + DL
36 arthrogryposis, distal, KG + DL
37 autoimmune disease of gastrointestinal tract KG + DL
38 action myoclonus-renal failure syndrome KG + DL
39 papillary meningioma of the cerebellum KG + DL
40 agammaglobulinemia KG + DL
41 Bacillaceae infectious disease KG + DL
42 bone dysplasia, lethal Holmgren type KG + DL
43 lymphocytic hypereosinophilic syndrome KG + DL
44 myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay KG + DL
45 pleural mesothelioma KG + DL
46 immunodeficiency-centromeric instability-facial anomalies syndrome KG + DL
47 neurohypophysis granular cell tumor KG + DL
48 hidrotic ectodermal dysplasia, Christianson-Fourie type KG + DL
49 lentivirus infection KG + DL
50 congenital nystagmus 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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