Phentermine

DrugBank ID: DB00191

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	3
DL Only	47
KG Only	0

Predictions

Indication	Score	Source
obesity disorder	0.9973	KG+DL
hypervitaminosis	0.9957	DL
proximal 16p11.2 microdeletion syndrome	0.9949	DL
obsolete hypertelorism (disease)	0.9941	DL
monogenic obesity	0.9920	KG+DL
frontorhiny	0.9904	DL
hypotensive disorder	0.9351	KG+DL
postural orthostatic tachycardia syndrome	0.8967	DL
lethal polymalformative syndrome, Boissel type	0.8066	DL
fatty liver disease	0.7774	DL
pentosuria	0.7497	DL
migraine with brainstem aura	0.7297	DL
migraine disorder	0.7096	DL
non-alcoholic steatohepatitis	0.6807	DL
hypercarotenemia and vitamin A deficiency, autosomal recessive	0.6553	DL
hypospadias 3, autosomal	0.6518	DL
sella turcica, bridged	0.6518	DL
triphalangeal thumb, Nonopposable	0.6518	DL
fibrosis of extraocular muscles, congenital, with synergistic divergence	0.6488	DL
variably protease-sensitive prionopathy	0.6439	DL
hyperparathyroidism, primary, caused by water clear cell hyperplasia	0.6390	DL
mitral valve prolapse, myxomatous	0.6256	DL
glaucoma with elevated episcleral venous pressure	0.6138	DL
hemangiomas of small intestine	0.6108	DL
retinal aplasia	0.6022	DL
hereditary persistence of alpha-fetoprotein	0.6004	DL
lattice degeneration of retina leading to retinal detachment	0.6003	DL
pancreas, dorsal, agenesis of	0.5960	DL
cholangiocarcinoma, susceptibility to	0.5942	DL
celiac artery stenosis from compression by median arcuate ligament of diaphragm	0.5935	DL
diarrhea 11, malabsorptive, congenital	0.5903	DL
multiple system atrophy	0.5898	DL
Tristichiasis	0.5896	DL
tarsal coalition	0.5883	DL
hyperemesis gravidarum (disease)	0.5883	DL
cornea plana 1, autosomal dominant	0.5882	DL
musk, inability to smell	0.5882	DL
polyhydramnios, chronic idiopathic	0.5882	DL
familial chronic myelocytic leukemia-like syndrome	0.5872	DL
central centrifugal cicatricial alopecia	0.5860	DL
cervical hypertrichosis with underlying kyphoscoliosis	0.5855	DL
factor VII and Factor VIII, combined deficiency of	0.5846	DL
pilonidal sinus (disease)	0.5844	DL
melanoma, malignant familial intraocular	0.5844	DL
prostate cancer, hereditary, X-linked	0.5843	DL
coxa vara (disease)	0.5834	DL
syncope, familial vasovagal	0.5831	DL
ocular cicatricial pemphigoid	0.5818	DL
lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis	0.5798	DL
ear folding	0.5792	DL

External Links

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