Triptorelin
DrugBank ID: DB06825
Summary
| Metric | Value |
|---|---|
| Total Predictions | 50 |
| KG+DL (Dual Validated) | 0 |
| DL Only | 50 |
| KG Only | 0 |
Predictions
| Indication | Score | Source |
|---|---|---|
| hypertrichosis (disease) | 1.0000 | DL |
| Ambras type hypertrichosis universalis congenita | 1.0000 | DL |
| malformation syndrome with odontal and/or periodontal component | 0.9999 | DL |
| syndrome with a Dandy-Walker malformation as major feature | 0.9999 | DL |
| isolated genetic hair shaft abnormality | 0.9999 | DL |
| allergic urticaria | 0.9991 | DL |
| familial male-limited precocious puberty | 0.9990 | DL |
| precocious puberty | 0.9989 | DL |
| familial isolated trichomegaly | 0.9988 | DL |
| aromatase excess syndrome | 0.9985 | DL |
| centra precocious puberty 1 | 0.9976 | DL |
| pelvic organ prolapse | 0.9967 | DL |
| female genital tuberculosis | 0.9965 | DL |
| physiological sexual disorder | 0.9965 | DL |
| cold urticaria | 0.9956 | DL |
| genetic alopecia | 0.9956 | DL |
| dysplasia of cervix | 0.9955 | DL |
| idiopathic central precocious puberty | 0.9944 | DL |
| renal-hepatic-pancreatic dysplasia | 0.9944 | DL |
| Joubert syndrome with renal defect | 0.9937 | DL |
| thoracic malformation | 0.9936 | DL |
| adult familial nephronophthisis-spastic quadriparesia syndrome | 0.9932 | DL |
| karyomegalic interstitial nephritis | 0.9918 | DL |
| subarachnoid hemorrhage (disease) | 0.9902 | DL |
| polycystic kidney disease 3 with or without polycystic liver disease | 0.9902 | DL |
| precocious puberty, central, 2 | 0.9899 | DL |
| nephrogenic syndrome of inappropriate antidiuresis | 0.9890 | DL |
| IgE responsiveness, atopic | 0.9883 | DL |
| pulmonary arterial hypertension | 0.9873 | DL |
| pulmonary arteriovenous malformation (disease) | 0.9872 | DL |
| polycystic kidney disease | 0.9872 | DL |
| recalcitrant atopic dermatitis | 0.9860 | DL |
| syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy | 0.9849 | DL |
| ACTH-independent macronodular adrenal hyperplasia | 0.9848 | DL |
| hypotrichosis simplex of the scalp | 0.9838 | DL |
| obsolete patella aplasia, coxa vara, and tarsal synostosis | 0.9833 | DL |
| sex differentiation disease | 0.9832 | DL |
| acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22) | 0.9826 | DL |
| gonadal disease | 0.9821 | DL |
| pulmonary arterial hypertension associated with congenital heart disease | 0.9813 | DL |
| persistent fetal circulation syndrome | 0.9810 | DL |
| familial clubfoot due to 17q23.1q23.2 microduplication | 0.9808 | DL |
| Cushing syndrome due to macronodular adrenal hyperplasia | 0.9803 | DL |
| diffuse alopecia areata | 0.9796 | DL |
| pulmonary arterial hypertension associated with HIV infection | 0.9792 | DL |
| pulmonary arterial hypertension associated with chronic hemolytic anemia | 0.9792 | DL |
| pulmonary arterial hypertension associated with connective tissue disease | 0.9792 | DL |
| pulmonary arterial hypertension associated with schistosomiasis | 0.9792 | DL |
| chromosome 17q23.1-q23.2 deletion syndrome | 0.9791 | DL |
| monostotic fibrous dysplasia (disease) | 0.9788 | 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.