Protamine Sulfate
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB09141 |
| 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 | intestinal hypomagnesemia 1 | KG + DL |
| 2 | Chuvash polycythemia | KG + DL |
| 3 | ring chromosome 14 | KG + DL |
| 4 | metaphyseal chondrodysplasia-retinitis pigmentosa syndrome | KG + DL |
| 5 | intrinsic factor and r binder, combined congenital deficiency of | KG + DL |
| 6 | neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination | KG + DL |
| 7 | Stankiewicz-Isidor syndrome | KG + DL |
| 8 | splenogonadal fusion-limb defects-micrognathia syndrome | KG + DL |
| 9 | oculo-auriculo-vertebral spectrum | KG + DL |
| 10 | Riley-Day syndrome | KG + DL |
| 11 | pericardial effusion, chronic | KG + DL |
| 12 | deoxyribose-5-phosphate aldolase deficiency | KG + DL |
| 13 | spondyloepiphyseal dysplasia tarda with characteristic facies | KG + DL |
| 14 | large congenital melanocytic nevus | KG + DL |
| 15 | odontochondrodysplasia | KG + DL |
| 16 | short chain acyl-CoA dehydrogenase deficiency | KG + DL |
| 17 | mismatch repair cancer syndrome | KG + DL |
| 18 | nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome | KG + DL |
| 19 | craniofacial anomalies and anterior segment dysgenesis syndrome | KG + DL |
| 20 | platelet storage pool deficiency | KG + DL |
| 21 | ossification of the posterior longitudinal ligament of the spine | KG + DL |
| 22 | neurodevelopmental disorder with central and peripheral motor dysfunction | KG + DL |
| 23 | congenital absence/hypoplasia of fingers or thumb | KG + DL |
| 24 | Pygmy | KG + DL |
| 25 | hemolytic anemia due to erythrocyte adenosine deaminase overproduction | KG + DL |
| 26 | platelet factor 3 deficiency | KG + DL |
| 27 | WHIM syndrome | KG + DL |
| 28 | short stature with nonspecific skeletal abnormalities | KG + DL |
| 29 | autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency | KG + DL |
| 30 | optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy | KG + DL |
| 31 | chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase | KG + DL |
| 32 | hypomyelination with brain stem and spinal cord involvement and leg spasticity | KG + DL |
| 33 | familial isolated hypoparathyroidism due to agenesis of parathyroid gland | KG + DL |
| 34 | polyglucosan body myopathy | KG + DL |
| 35 | kapur-Toriello syndrome | KG + DL |
| 36 | otodental syndrome | KG + DL |
| 37 | granulosis rubra nasi | KG + DL |
| 38 | hepatoencephalopathy due to combined oxidative phosphorylation defect type 1 | KG + DL |
| 39 | orotic aciduria | KG + DL |
| 40 | autosomal dominant Robinow syndrome | KG + DL |
| 41 | early-onset generalized dystonia | KG + DL |
| 42 | FRAXE intellectual disability | KG + DL |
| 43 | rhabdoid tumor predisposition syndrome | KG + DL |
| 44 | Blount disease, infantile | KG + DL |
| 45 | complement factor I deficiency | KG + DL |
| 46 | thrombomodulin-related bleeding disorder | KG + DL |
| 47 | Rajab interstitial lung disease with brain calcifications | KG + DL |
| 48 | Say-field-Coldwell syndrome | KG + DL |
| 49 | megalocornea (disease) | KG + DL |
| 50 | BENTA disease | 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.