| Item | Value |
|---|---|
| DrugBank ID | DB00624 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 1290 |
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | hypogonadotropic hypogonadism with or without anosmia | TxGNN Knowledge Graph |
| 2 | acquired pituitary hormone deficiency | TxGNN Knowledge Graph |
| 3 | pituitary deficiency due to empty sella turcica syndrome | TxGNN Knowledge Graph |
| 4 | pituitary deficiency | TxGNN Knowledge Graph |
| 5 | hypogonadism, male | TxGNN Knowledge Graph |
| 6 | hypogonadism | TxGNN Knowledge Graph |
| 7 | X-linked intellectual disability with isolated growth hormone deficiency | TxGNN Knowledge Graph |
| 8 | isolated growth hormone deficiency | TxGNN Knowledge Graph |
| 9 | pituitary hormone defiency from vascular origin | TxGNN Knowledge Graph |
| 10 | isolated congenital growth hormone deficiency | TxGNN Knowledge Graph |
| 11 | non-acquired combined pituitary hormone deficiency | TxGNN Knowledge Graph |
| 12 | congenital hypogonadotropic hypogonadism | TxGNN Knowledge Graph |
| 13 | short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia | TxGNN Knowledge Graph |
| 14 | Klinefelter syndrome | TxGNN Knowledge Graph |
| 15 | hypopituitarism | TxGNN Knowledge Graph |
| 16 | pituitary deficiency due to Rathke’s pouch cysts | TxGNN Knowledge Graph |
| 17 | thymus gland disease | TxGNN Knowledge Graph |
| 18 | non-acquired combined pituitary hormone deficiencies without extra-pituitary malformations | TxGNN Knowledge Graph |
| 19 | Sheehan syndrome | TxGNN Knowledge Graph |
| 20 | androgen insensitivity syndrome | TxGNN Knowledge Graph |
| 21 | Kallmann syndrome | TxGNN Knowledge Graph |
| 22 | trisomy 13 | TxGNN Knowledge Graph |
| 23 | hypogonadotropic hypogonadism | TxGNN Knowledge Graph |
| 24 | eunuchism | TxGNN Knowledge Graph |
| 25 | combined pituitary hormone deficiencies, genetic form | TxGNN Knowledge Graph |
| 26 | hypogonadotropic hypogonadism-frontoparietal alopecia syndrome | TxGNN Knowledge Graph |
| 27 | cryptorchidism (disease) | TxGNN Knowledge Graph |
| 28 | short stature due to growth hormone qualitative anomaly | TxGNN Knowledge Graph |
| 29 | non-acquired pituitary hormone deficiency | TxGNN Knowledge Graph |
| 30 | premature menopause | TxGNN Knowledge Graph |
| 31 | hypogonadotropic hypogonadism with or without anosmia | TxGNN Knowledge Graph |
| 32 | acquired pituitary hormone deficiency | TxGNN Knowledge Graph |
| 33 | pituitary deficiency due to empty sella turcica syndrome | TxGNN Knowledge Graph |
| 34 | pituitary deficiency | TxGNN Knowledge Graph |
| 35 | hypogonadism, male | TxGNN Knowledge Graph |
| 36 | hypogonadism | TxGNN Knowledge Graph |
| 37 | X-linked intellectual disability with isolated growth hormone deficiency | TxGNN Knowledge Graph |
| 38 | isolated growth hormone deficiency | TxGNN Knowledge Graph |
| 39 | pituitary hormone defiency from vascular origin | TxGNN Knowledge Graph |
| 40 | isolated congenital growth hormone deficiency | TxGNN Knowledge Graph |
| 41 | non-acquired combined pituitary hormone deficiency | TxGNN Knowledge Graph |
| 42 | congenital hypogonadotropic hypogonadism | TxGNN Knowledge Graph |
| 43 | short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia | TxGNN Knowledge Graph |
| 44 | Klinefelter syndrome | TxGNN Knowledge Graph |
| 45 | hypopituitarism | TxGNN Knowledge Graph |
| 46 | pituitary deficiency due to Rathke’s pouch cysts | TxGNN Knowledge Graph |
| 47 | thymus gland disease | TxGNN Knowledge Graph |
| 48 | non-acquired combined pituitary hormone deficiencies without extra-pituitary malformations | TxGNN Knowledge Graph |
| 49 | Sheehan syndrome | TxGNN Knowledge Graph |
| 50 | androgen insensitivity syndrome | TxGNN Knowledge Graph |
(Showing top 50 of 1290 predictions)
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.