Degarelix

Basic Information

Item Value
DrugBank ID DB06699
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 71

Predicted Indications (TxGNN)

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

# Indication Source
1 hypertrichosis (disease) KG + DL
2 Ambras type hypertrichosis universalis congenita KG + DL
3 syndrome with a Dandy-Walker malformation as major feature KG + DL
4 malformation syndrome with odontal and/or periodontal component KG + DL
5 isolated genetic hair shaft abnormality KG + DL
6 allergic urticaria KG + DL
7 cold urticaria KG + DL
8 familial male-limited precocious puberty KG + DL
9 centra precocious puberty 1 KG + DL
10 familial isolated trichomegaly KG + DL
11 precocious puberty KG + DL
12 Plasmodium falciparum malaria KG + DL
13 nephrogenic syndrome of inappropriate antidiuresis KG + DL
14 aromatase excess syndrome KG + DL
15 IgE responsiveness, atopic KG + DL
16 recalcitrant atopic dermatitis KG + DL
17 subarachnoid hemorrhage (disease) KG + DL
18 renal-hepatic-pancreatic dysplasia KG + DL
19 thoracic malformation KG + DL
20 adult familial nephronophthisis-spastic quadriparesia syndrome KG + DL
21 Joubert syndrome with renal defect KG + DL
22 pelvic organ prolapse KG + DL
23 physiological sexual disorder KG + DL
24 female genital tuberculosis KG + DL
25 karyomegalic interstitial nephritis KG + DL
26 multidrug-resistant tuberculosis KG + DL
27 dysplasia of cervix KG + DL
28 polycystic kidney disease 3 with or without polycystic liver disease KG + DL
29 idiopathic central precocious puberty KG + DL
30 polycystic kidney disease KG + DL
31 tuberculosis, avian KG + DL
32 tuberculous ascites KG + DL
33 tuberculoma KG + DL
34 inactive tuberculosis KG + DL
35 tuberculosis, bovine KG + DL
36 acquired aneurysmal subarachnoid hemorrhage KG + DL
37 malaria KG + DL
38 acute intermittent porphyria KG + DL
39 duodenal obstruction KG + DL
40 acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) KG + DL
41 duodenogastric reflux KG + DL
42 syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy KG + DL
43 precocious puberty, central, 2 KG + DL
44 duodenal ulcer (disease) KG + DL
45 ACTH-independent macronodular adrenal hyperplasia KG + DL
46 urticaria, aquagenic KG + DL
47 autoimmune urticaria KG + DL
48 angioedema KG + DL
49 genetic alopecia KG + DL
50 epulis KG + DL

(Showing top 50 of 71 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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