Isoleucine

Basic Information

Item Value
DrugBank ID DB00167
Evidence Level L5 (Computational Prediction)
Number of Predicted Indications 35

Predicted Indications (TxGNN)

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

# Indication Source
1 gastroparesis (disease) KG + DL
2 obsolete vitamin D deficiency KG + DL
3 congenital prothrombin deficiency KG + DL
4 dyspepsia KG + DL
5 renal tubular acidosis KG + DL
6 sclerosing cholangitis KG + DL
7 familial visceral myopathy KG + DL
8 hypophosphatemic rickets KG + DL
9 potassium deficiency disease KG + DL
10 myopathic intestinal pseudoobstruction KG + DL
11 unclassified intestinal pseudoobstruction KG + DL
12 intestinal obstruction KG + DL
13 albinism-deafness syndrome KG + DL
14 familial isolated hypoparathyroidism due to impaired PTH secretion KG + DL
15 neuronal intestinal dysplasia, type B KG + DL
16 acromesomelic dysplasia, Campailla Martinelli type KG + DL
17 postmenopausal osteoporosis KG + DL
18 craniofacial conodysplasia KG + DL
19 Dahlberg-Borer-Newcomer syndrome KG + DL
20 pregnancy associated osteoporosis KG + DL
21 postgastrectomy syndrome KG + DL
22 primary hereditary glaucoma KG + DL
23 hypoparathyroidism KG + DL
24 succinyl-CoA:3-ketoacid CoA transferase deficiency KG + DL
25 vitamin deficiency disorder KG + DL
26 autosomal dominant neovascular inflammatory vitreoretinopathy KG + DL
27 Worth syndrome KG + DL
28 stomach disease KG + DL
29 Alstrom syndrome KG + DL
30 Pendred syndrome KG + DL
31 hereditary hypophosphatemic rickets KG + DL
32 open-angle glaucoma KG + DL
33 acne (disease) KG + DL
34 intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked KG + DL
35 biotin metabolic disease KG + DL

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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