Ganirelix

DrugBank ID: DB06785

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	0
DL Only	50
KG Only	0

Predictions

Indication	Score	Source
hypertrichosis (disease)	0.9998	DL
Ambras type hypertrichosis universalis congenita	0.9998	DL
malformation syndrome with odontal and/or periodontal component	0.9997	DL
syndrome with a Dandy-Walker malformation as major feature	0.9997	DL
isolated genetic hair shaft abnormality	0.9997	DL
familial male-limited precocious puberty	0.9985	DL
persistent fetal circulation syndrome	0.9980	DL
aromatase excess syndrome	0.9980	DL
centra precocious puberty 1	0.9975	DL
familial isolated trichomegaly	0.9975	DL
pelvic organ prolapse	0.9962	DL
female genital tuberculosis	0.9960	DL
physiological sexual disorder	0.9960	DL
idiopathic central precocious puberty	0.9959	DL
dysplasia of cervix	0.9950	DL
X-linked congenital generalized hypertrichosis	0.9950	DL
precocious puberty, central, 2	0.9945	DL
diffuse cutaneous mastocytosis	0.9942	DL
genetic alopecia	0.9938	DL
precocious puberty	0.9931	DL
amenorrhea (disease)	0.9919	DL
ACTH-independent macronodular adrenal hyperplasia	0.9897	DL
Cushing syndrome due to macronodular adrenal hyperplasia	0.9889	DL
isolated congenital growth hormone deficiency	0.9889	DL
gonadal disease	0.9872	DL
pulmonary arteriovenous malformation (disease)	0.9866	DL
pulmonary arterial hypertension	0.9855	DL
monostotic fibrous dysplasia (disease)	0.9855	DL
habitual spontaneous abortion	0.9846	DL
polyostotic fibrous dysplasia	0.9839	DL
sex differentiation disease	0.9830	DL
allergic urticaria	0.9808	DL
pulmonary arterial hypertension associated with congenital heart disease	0.9806	DL
pulmonary arterial hypertension associated with HIV infection	0.9795	DL
pulmonary arterial hypertension associated with chronic hemolytic anemia	0.9795	DL
pulmonary arterial hypertension associated with connective tissue disease	0.9795	DL
pulmonary arterial hypertension associated with schistosomiasis	0.9795	DL
non-syndromic brachydactyly	0.9783	DL
pituitary dwarfism	0.9774	DL
renal-hepatic-pancreatic dysplasia	0.9751	DL
familial clubfoot due to 17q23.1q23.2 microduplication	0.9749	DL
syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy	0.9748	DL
obsolete patella aplasia, coxa vara, and tarsal synostosis	0.9746	DL
coxopodopatellar syndrome	0.9739	DL
Joubert syndrome with renal defect	0.9737	DL
chromosome 17q23.1-q23.2 deletion syndrome	0.9731	DL
adrenocortical insufficiency	0.9731	DL
persistent Mullerian duct syndrome	0.9728	DL
precocious puberty in female	0.9723	DL
pituitary hormone deficiency, combined	0.9723	DL

External Links

Disclaimer
Predictions are for research purposes only and do not constitute medical advice.