Cetrorelix

Basic Information

Item Value
DrugBank ID DB00050
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 hypertrichosis (disease) KG + DL
2 Ambras type hypertrichosis universalis congenita KG + DL
3 malformation syndrome with odontal and/or periodontal component KG + DL
4 syndrome with a Dandy-Walker malformation as major feature KG + DL
5 isolated genetic hair shaft abnormality KG + DL
6 persistent fetal circulation syndrome KG + DL
7 familial isolated trichomegaly KG + DL
8 familial male-limited precocious puberty KG + DL
9 aromatase excess syndrome KG + DL
10 centra precocious puberty 1 KG + DL
11 pelvic organ prolapse KG + DL
12 female genital tuberculosis KG + DL
13 physiological sexual disorder KG + DL
14 genetic alopecia KG + DL
15 X-linked congenital generalized hypertrichosis KG + DL
16 idiopathic central precocious puberty KG + DL
17 diffuse cutaneous mastocytosis KG + DL
18 dysplasia of cervix KG + DL
19 precocious puberty, central, 2 KG + DL
20 amenorrhea (disease) KG + DL
21 precocious puberty KG + DL
22 allergic urticaria KG + DL
23 isolated congenital growth hormone deficiency KG + DL
24 ACTH-independent macronodular adrenal hyperplasia KG + DL
25 pulmonary arteriovenous malformation (disease) KG + DL
26 Cushing syndrome due to macronodular adrenal hyperplasia KG + DL
27 pulmonary arterial hypertension KG + DL
28 gonadal disease KG + DL
29 monostotic fibrous dysplasia (disease) KG + DL
30 pulmonary arterial hypertension associated with congenital heart disease KG + DL
31 habitual spontaneous abortion KG + DL
32 pulmonary arterial hypertension associated with schistosomiasis KG + DL
33 pulmonary arterial hypertension associated with HIV infection KG + DL
34 pulmonary arterial hypertension associated with chronic hemolytic anemia KG + DL
35 pulmonary arterial hypertension associated with connective tissue disease KG + DL
36 polyostotic fibrous dysplasia KG + DL
37 syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy KG + DL
38 non-syndromic brachydactyly KG + DL
39 adrenocortical insufficiency KG + DL
40 candidiasis KG + DL
41 IgE responsiveness, atopic KG + DL
42 pituitary dwarfism KG + DL
43 familial adrenal hypoplasia with absent pituitary luteinizing hormone KG + DL
44 hypotrichosis simplex of the scalp KG + DL
45 sex differentiation disease KG + DL
46 recalcitrant atopic dermatitis KG + DL
47 PAGOD syndrome KG + DL
48 diffuse alopecia areata KG + DL
49 cold urticaria KG + DL
50 46,XY disorder of sex development 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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