Methyldopa
DrugBank ID: DB00968
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 1 |
| DL Only | 49 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| malignant hypertensive renal disease | 0.9663 | DL |
| malignant renovascular hypertension | 0.9663 | DL |
| hypertensive disorder | 0.9638 | KG+DL |
| pulmonary hypertension owing to lung disease and/or hypoxia | 0.9630 | DL |
| pulmonary hypertension with unclear multifactorial mechanism | 0.9630 | DL |
| Braddock syndrome | 0.9511 | DL |
| chronic pulmonary heart disease | 0.8503 | DL |
| congenital temporomandibular joint ankylosis | 0.5750 | DL |
| polydipsia | 0.5718 | DL |
| atrial flutter (disease) | 0.5666 | DL |
| anuria | 0.5665 | DL |
| cholangiocarcinoma, susceptibility to | 0.5618 | DL |
| obsolete superimposed infection | 0.5388 | DL |
| obsolete left bundle branch block | 0.5373 | DL |
| tibial adamantinoma | 0.5370 | DL |
| conduct disorder | 0.5326 | DL |
| ocular tuberculosis | 0.5325 | DL |
| sudden arrhythmia death syndrome | 0.5292 | DL |
| mitral valve prolapse, myxomatous | 0.5284 | DL |
| ergotism | 0.5281 | DL |
| cloacogenic carcinoma | 0.5225 | DL |
| spinal chordoma | 0.5204 | DL |
| hypercarotenemia and vitamin A deficiency, autosomal recessive | 0.5204 | DL |
| obsolete functional visual loss | 0.5186 | DL |
| pulmonary valve insufficiency | 0.5182 | DL |
| obsolete pathologic fracture | 0.5168 | DL |
| Marin-Amat syndrome | 0.5168 | DL |
| inverse Marcus-Gunn phenomenon | 0.5168 | DL |
| urinary tract obstruction | 0.5157 | DL |
| sunburn | 0.5143 | DL |
| epidural abscess | 0.5137 | DL |
| congenital cystic eye multiple ocular and intracranial anomalies | 0.5130 | DL |
| obsolete breast fibroadenosis | 0.5109 | DL |
| hypermobility syndrome | 0.5083 | DL |
| arteriosclerosis obliterans | 0.5060 | DL |
| paramedian facial cleft | 0.5060 | DL |
| recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome | 0.5036 | DL |
| nonarteritic anterior ischemic optic neuropathy, susceptibility to | 0.5024 | DL |
| prosopagnosia (disease) | 0.5010 | DL |
| SELENON-related myopathy | 0.5000 | DL |
| X inactivation, familial skewed | 0.5000 | DL |
| febrile seizures plus, genetic epilepsy with febrile seizures plus | 0.5000 | DL |
| hearing loss with skin disease | 0.5000 | DL |
| hypereosinophilia of undetermined significance | 0.5000 | DL |
| hyperkalemic renal tubular acidosis | 0.5000 | DL |
| hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses | 0.5000 | DL |
| lymphoma, Hodgkin, X-linked pseudoautosomal | 0.5000 | DL |
| methicillin-resistant staphylococcus aureus infectious disease | 0.5000 | DL |
| pneumoconiosis due to talc | 0.5000 | DL |
| seminal vesicle chronic gonorrhea | 0.5000 | DL |
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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.