Aprepitant
DrugBank ID: DB00673
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| nephrogenic syndrome of inappropriate antidiuresis | 0.9997 | DL |
| hypertrichosis (disease) | 0.9991 | DL |
| pulmonary hypertension | 0.9990 | DL |
| leprosy | 0.9990 | DL |
| Ambras type hypertrichosis universalis congenita | 0.9987 | DL |
| malformation syndrome with odontal and/or periodontal component | 0.9986 | DL |
| kyphoscoliotic heart disease | 0.9986 | DL |
| syndrome with a Dandy-Walker malformation as major feature | 0.9986 | DL |
| subarachnoid hemorrhage (disease) | 0.9985 | DL |
| isolated genetic hair shaft abnormality | 0.9985 | DL |
| persistent Mullerian duct syndrome | 0.9963 | DL |
| multiple endocrine neoplasia | 0.9961 | DL |
| nephrogenic diabetes insipidus | 0.9947 | DL |
| pulmonary hypertension, primary, autosomal recessive | 0.9942 | DL |
| obsolete patella aplasia, coxa vara, and tarsal synostosis | 0.9939 | DL |
| chromosome 17q23.1-q23.2 deletion syndrome | 0.9928 | DL |
| familial clubfoot due to 17q23.1q23.2 microduplication | 0.9928 | DL |
| acquired aneurysmal subarachnoid hemorrhage | 0.9926 | DL |
| coxopodopatellar syndrome | 0.9924 | DL |
| hypoalphalipoproteinemia | 0.9919 | DL |
| pneumocystosis | 0.9918 | DL |
| homozygous familial hypercholesterolemia | 0.9917 | DL |
| Cryptococcal meningitis | 0.9909 | DL |
| acute neonatal citrullinemia type I | 0.9899 | DL |
| adult-onset citrullinemia type I | 0.9899 | DL |
| thoracic malformation | 0.9899 | DL |
| hyperargininemia | 0.9898 | DL |
| Jeune syndrome | 0.9897 | DL |
| adult familial nephronophthisis-spastic quadriparesia syndrome | 0.9891 | DL |
| renal-hepatic-pancreatic dysplasia | 0.9885 | DL |
| karyomegalic interstitial nephritis | 0.9880 | DL |
| idiopathic pulmonary arterial hypertension | 0.9877 | DL |
| mitochondrial DNA depletion syndrome, hepatocerebrorenal form | 0.9876 | DL |
| polycystic kidney disease | 0.9875 | DL |
| hereditary renal hypouricemia | 0.9869 | DL |
| benign prostatic hyperplasia (disease) | 0.9869 | DL |
| pulmonary hypertension, primary | 0.9868 | DL |
| common cold | 0.9868 | DL |
| Joubert syndrome with renal defect | 0.9863 | DL |
| cor pulmonale | 0.9860 | DL |
| idiopathic and/or familial pulmonary arterial hypertension | 0.9860 | DL |
| intracranial abscess | 0.9852 | DL |
| familial isolated trichomegaly | 0.9847 | DL |
| urea cycle disorder | 0.9845 | DL |
| polycystic kidney disease 3 with or without polycystic liver disease | 0.9843 | DL |
| migraine disorder | 0.9837 | DL |
| retinitis | 0.9830 | DL |
| gastrointestinal hamartoma | 0.9828 | DL |
| motor nerve neuritis | 0.9824 | DL |
| Senior-Boichis syndrome | 0.9822 | DL |
External Links
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.