Acetazolamide
DrugBank ID: DB00819
Summary
| Metric | Value |
|---|---|
| Total Predictions | 52 |
| KG+DL (Dual Validated) | 1 |
| DL Only | 49 |
| KG Only | 2 |
Predictions
| Indication | Score | Source |
|---|---|---|
| exercise-induced malignant hyperthermia | 0.9995 | DL |
| hypertrophic cardiomyopathy | 0.9993 | DL |
| congenital myopathy with excess of thin filaments | 0.9990 | DL |
| hypertrophic cardiomyopathy due to intensive athletic training | 0.9989 | DL |
| distal myopathy, Tateyama type | 0.9988 | DL |
| cirrhotic cardiomyopathy | 0.9988 | DL |
| cardiomyopathy | 0.9983 | DL |
| intestinal obstruction | 0.9982 | DL |
| glycogen storage disease due to acid maltase deficiency, late-onset | 0.9980 | DL |
| myopathic intestinal pseudoobstruction | 0.9979 | DL |
| unclassified intestinal pseudoobstruction | 0.9979 | DL |
| familial hypertrophic cardiomyopathy | 0.9977 | DL |
| neuronal intestinal dysplasia, type B | 0.9976 | DL |
| familial isolated arrhythmogenic ventricular dysplasia | 0.9973 | DL |
| familial visceral myopathy | 0.9972 | DL |
| disorder of fatty acid oxidation and ketogenesis | 0.9970 | DL |
| glycogen storage disease due to glycogen branching enzyme deficiency | 0.9969 | DL |
| familial periodic paralysis | 0.9968 | DL |
| malignant hyperthermia, susceptibility to | 0.9958 | DL |
| closed-angle glaucoma | 0.9957 | DL |
| hypokalemic periodic paralysis | 0.9957 | DL |
| endomyocardial fibrosis | 0.9954 | DL |
| carnitine-acylcarnitine translocase deficiency | 0.9950 | DL |
| trigeminal nerve neoplasm | 0.9947 | DL |
| moderate multiminicore disease with hand involvement | 0.9940 | DL |
| malignant hyperthermia of anesthesia | 0.9932 | DL |
| congenital multicore myopathy with external ophthalmoplegia | 0.9929 | DL |
| thyrotoxic periodic paralysis, susceptibility to | 0.9924 | DL |
| familial dilated cardiomyopathy | 0.9924 | DL |
| central core myopathy | 0.9924 | DL |
| mitochondrial DNA depletion syndrome 12a (cardiomyopathic type), autosomal dominant | 0.9919 | DL |
| thyrotoxic periodic paralysis | 0.9916 | DL |
| methemoglobinemia due to deficiency of methemoglobin reductase | 0.9916 | DL |
| King-Denborough syndrome | 0.9908 | DL |
| intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked | 0.9907 | DL |
| neuronal intestinal pseudoobstruction | 0.9905 | DL |
| angle-closure glaucoma | 0.9902 | DL |
| absence epilepsy | 0.9896 | KG+DL |
| methemoglobinemia, alpha type | 0.9889 | DL |
| dilated cardiomyopathy | 0.9882 | DL |
| gastroparesis (disease) | 0.9882 | DL |
| obsolete bundle branch block | 0.9875 | DL |
| aqueous misdirection | 0.9858 | DL |
| traumatic glaucoma | 0.9858 | DL |
| glaucomatous atrophy of optic disc | 0.9848 | DL |
| methemoglobin reductase deficiency | 0.9839 | DL |
| complex neurodevelopmental disorder | 0.9835 | DL |
| neovascular glaucoma | 0.9834 | DL |
| myopathy, centronuclear | 0.9832 | DL |
| pyruvate dehydrogenase E3 deficiency | 0.9828 | DL |
Showing top 50 of 52 predictions.
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Disclaimer
Predictions are for research purposes only and do not constitute medical advice.
Predictions are for research purposes only and do not constitute medical advice.