Somatostatin

DrugBank ID: DB09099

Summary

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

Predictions

Indication	Score	Source
amenorrhea (disease)	0.9864	DL
Leydig cell hypoplasia due to LH resistance	0.9766	DL
46,XY disorder of sex development due to impaired androgen production	0.9748	DL
hypogonadotropic hypogonadism with or without anosmia	0.9652	DL
multiple endocrine neoplasia	0.9566	DL
mycotic corneal ulcer	0.9532	DL
pulmonary hypertension	0.9514	DL
kyphoscoliotic heart disease	0.9475	DL
HER2 positive breast carcinoma	0.9444	DL
homozygous familial hypercholesterolemia	0.9440	DL
Ambras type hypertrichosis universalis congenita	0.9434	DL
malformation syndrome with odontal and/or periodontal component	0.9428	DL
hypertrichosis (disease)	0.9417	DL
syndrome with a Dandy-Walker malformation as major feature	0.9381	DL
isolated genetic hair shaft abnormality	0.9363	DL
candidiasis	0.9352	DL
progesterone-receptor negative breast cancer	0.9257	DL
normal breast-like subtype of breast carcinoma	0.9253	DL
progesterone-receptor positive breast cancer	0.9253	DL
breast tumor luminal A or B	0.9236	DL
adrenal gland hyperfunction	0.9223	DL
migraine disorder	0.9151	DL
infectious bovine rhinotracheitis	0.9150	DL
malignant catarrh	0.9150	DL
migraine with brainstem aura	0.9144	DL
cytomegalovirus infection	0.9127	DL
oral candidiasis	0.9046	DL
acne (disease)	0.8984	DL
osteoradionecrosis of the mandible	0.8949	DL
commissural lip fistula	0.8944	DL
burning mouth syndrome	0.8929	DL
oral leukoedema	0.8929	DL
obsolete patella aplasia, coxa vara, and tarsal synostosis	0.8919	DL
acromelanosis	0.8915	DL
congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome	0.8915	DL
leprosy	0.8913	DL
leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome	0.8912	DL
coxopodopatellar syndrome	0.8874	DL
familial generalized lentiginosis	0.8870	DL
rhabdoid tumor	0.8857	DL
hereditary neuroendocrine tumor of small intestine	0.8844	DL
pulmonary hypertension, primary, autosomal recessive	0.8832	DL
peripheral nerve schwannoma	0.8830	DL
familial clubfoot due to 17q23.1q23.2 microduplication	0.8806	DL
gastrocutaneous syndrome	0.8803	DL
osteopathia striata-pigmentary dermopathy-white forelock syndrome	0.8801	DL
chromosome 17q23.1-q23.2 deletion syndrome	0.8784	DL
progeria-short stature-pigmented nevi syndrome	0.8781	DL
idiopathic pulmonary arterial hypertension	0.8772	DL
progeroid syndrome, Petty type	0.8749	DL

External Links

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