Memantine Hcl
Basic Information
| Item | Value |
|---|---|
| DrugBank ID | DB01043 |
| Evidence Level | L5 (Computational Prediction) |
| Number of Predicted Indications | 98 |
Predicted Indications (TxGNN)
The following are potential new indications predicted by the TxGNN model. Higher scores indicate higher predicted relevance.
| # | Indication | Source |
|---|---|---|
| 1 | pulmonary hypertension | KG + DL |
| 2 | migraine disorder | KG + DL |
| 3 | kyphoscoliotic heart disease | KG + DL |
| 4 | migraine with brainstem aura | KG + DL |
| 5 | rheumatoid arthritis | KG + DL |
| 6 | nephrogenic syndrome of inappropriate antidiuresis | KG + DL |
| 7 | atrophoderma vermiculata | KG + DL |
| 8 | migraine with or without aura, susceptibility to | KG + DL |
| 9 | ulerythema ophryogenesis | KG + DL |
| 10 | brachydactyly-syndactyly syndrome | KG + DL |
| 11 | osteoarthritis susceptibility | KG + DL |
| 12 | colobomatous microphthalmia-rhizomelic dysplasia syndrome | KG + DL |
| 13 | tendinitis | KG + DL |
| 14 | pulmonary hypertension, primary, autosomal recessive | KG + DL |
| 15 | gout | KG + DL |
| 16 | myositis fibrosa | KG + DL |
| 17 | idiopathic granulomatous myositis | KG + DL |
| 18 | fibromyalgia | KG + DL |
| 19 | obsolete patella aplasia, coxa vara, and tarsal synostosis | KG + DL |
| 20 | multiple endocrine neoplasia | KG + DL |
| 21 | cor pulmonale | KG + DL |
| 22 | inclusion body myositis | KG + DL |
| 23 | neuroretinitis | KG + DL |
| 24 | vestibular neuronitis | KG + DL |
| 25 | familial clubfoot due to 17q23.1q23.2 microduplication | KG + DL |
| 26 | chromosome 17q23.1-q23.2 deletion syndrome | KG + DL |
| 27 | Smouldering systemic mastocytosis | KG + DL |
| 28 | hypotrichosis simplex of the scalp | KG + DL |
| 29 | brachial plexus neuritis | KG + DL |
| 30 | systemic mastocytosis | KG + DL |
| 31 | congenital hypotrichosis milia | KG + DL |
| 32 | coxopodopatellar syndrome | KG + DL |
| 33 | motor nerve neuritis | KG + DL |
| 34 | diffuse alopecia areata | KG + DL |
| 35 | lymphoadenopathic mastocytosis with eosinophilia | KG + DL |
| 36 | alopecia | KG + DL |
| 37 | idiopathic and/or familial pulmonary arterial hypertension | KG + DL |
| 38 | acute pulmonary heart disease | KG + DL |
| 39 | congestive heart failure | KG + DL |
| 40 | acromesomelic dysplasia, Hunter-Thompson type | KG + DL |
| 41 | idiopathic pulmonary arterial hypertension | KG + DL |
| 42 | pulmonary hypertension, primary | KG + DL |
| 43 | Tourette syndrome | KG + DL |
| 44 | osteoarthritis | KG + DL |
| 45 | methemoglobinemia, alpha type | KG + DL |
| 46 | homozygous familial hypercholesterolemia | KG + DL |
| 47 | brachyolmia | KG + DL |
| 48 | trichotillomania | KG + DL |
| 49 | chronic pulmonary heart disease | KG + DL |
| 50 | methemoglobinemia | KG + DL |
(Showing top 50 of 98 predictions)
Disclaimer
These predictions are for research purposes only and do not constitute medical advice. Clinical validation is required before any clinical application.