Nitrogen
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB09152 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 61 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | 16q24.1 microdeletion syndrome | KG + DL |
| 2 | primary interstitial lung disease specific to childhood | KG + DL |
| 3 | isolated pulmonary capillaritis | KG + DL |
| 4 | congenital pulmonary lymphangiectasia | KG + DL |
| 5 | benign neoplasm of adrenal gland | KG + DL |
| 6 | malformation syndrome with odontal and/or periodontal component | KG + DL |
| 7 | syndrome with a Dandy-Walker malformation as major feature | KG + DL |
| 8 | isolated genetic hair shaft abnormality | KG + DL |
| 9 | Ambras type hypertrichosis universalis congenita | KG + DL |
| 10 | hypertrichosis (disease) | KG + DL |
| 11 | mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies | KG + DL |
| 12 | autosomal ichthyosis syndrome with fatal disease course | KG + DL |
| 13 | pulmonary arteriovenous malformation (disease) | KG + DL |
| 14 | Gaucher disease | KG + DL |
| 15 | Steel syndrome | KG + DL |
| 16 | pulmonary arterial hypertension associated with congenital heart disease | KG + DL |
| 17 | pulmonary arterial hypertension associated with HIV infection | KG + DL |
| 18 | pulmonary arterial hypertension associated with schistosomiasis | KG + DL |
| 19 | pulmonary arterial hypertension associated with connective tissue disease | KG + DL |
| 20 | pulmonary arterial hypertension associated with chronic hemolytic anemia | KG + DL |
| 21 | hypophosphatasia | KG + DL |
| 22 | citrullinemia, type II, adult-onset | KG + DL |
| 23 | adult-onset citrullinemia type I | KG + DL |
| 24 | acute neonatal citrullinemia type I | KG + DL |
| 25 | Hurler syndrome | KG + DL |
| 26 | polycystic kidney disease 3 with or without polycystic liver disease | KG + DL |
| 27 | citrin deficiency | KG + DL |
| 28 | Cushing disease due to pituitary adenoma | KG + DL |
| 29 | renal-hepatic-pancreatic dysplasia | KG + DL |
| 30 | exocrine pancreatic insufficiency | KG + DL |
| 31 | Joubert syndrome with renal defect | KG + DL |
| 32 | pituitary dwarfism | KG + DL |
| 33 | pulmonary arterial hypertension | KG + DL |
| 34 | thoracic malformation | KG + DL |
| 35 | karyomegalic interstitial nephritis | KG + DL |
| 36 | monosomy X | KG + DL |
| 37 | syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy | KG + DL |
| 38 | adult familial nephronophthisis-spastic quadriparesia syndrome | KG + DL |
| 39 | Gaucher disease perinatal lethal | KG + DL |
| 40 | growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant | KG + DL |
| 41 | lysosomal storage disease with skeletal involvement | KG + DL |
| 42 | adult Krabbe disease | KG + DL |
| 43 | congenital anomaly of the great veins | KG + DL |
| 44 | Tay-Sachs disease | KG + DL |
| 45 | Scheie syndrome | KG + DL |
| 46 | cholesterol metabolism disease | KG + DL |
| 47 | primary bone dysplasia with increased bone density | KG + DL |
| 48 | Krabbe disease | KG + DL |
| 49 | autosomal dominant polycystic liver disease | KG + DL |
| 50 | metachromatic leukodystrophy | KG + DL |
(Showing top 50 of 61 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.