Pemigatinib

DrugBank ID: DB15102

Summary

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

Predictions

Indication	Score	Source
multiple endocrine neoplasia	0.9971	DL
amenorrhea (disease)	0.9954	DL
HER2 positive breast carcinoma	0.9949	DL
cytomegalovirus infection	0.9946	DL
infectious bovine rhinotracheitis	0.9943	DL
malignant catarrh	0.9943	DL
amyotrophic lateral sclerosis	0.9941	DL
amyotrohpic lateral sclerosis type 22	0.9927	DL
amyotrophic lateral sclerosis, susceptibility to	0.9925	DL
axial spondylometaphyseal dysplasia	0.9925	DL
Mills syndrome	0.9922	DL
progesterone-receptor negative breast cancer	0.9918	DL
normal breast-like subtype of breast carcinoma	0.9917	DL
progesterone-receptor positive breast cancer	0.9917	DL
trichomegaly-retina pigmentary degeneration-dwarfism syndrome	0.9917	DL
breast tumor luminal A or B	0.9915	DL
lethal arthrogryposis-anterior horn cell disease syndrome	0.9912	DL
bilateral parasagittal parieto-occipital polymicrogyria	0.9909	DL
lower motor neuron syndrome with late-adult onset	0.9908	DL
monomelic amyotrophy	0.9903	DL
hypoalphalipoproteinemia	0.9893	DL
autosomal dominant mitochondrial myopathy with exercise intolerance	0.9892	DL
hereditary neuroendocrine tumor of small intestine	0.9862	DL
homozygous familial hypercholesterolemia	0.9858	DL
HIV infectious disease	0.9841	DL
thrombocytopenia	0.9810	DL
feline acquired immunodeficiency syndrome	0.9802	DL
simian immunodeficiency virus infection	0.9802	DL
acne (disease)	0.9801	DL
marcothrombocytopenia with mitral valve insufficiency	0.9799	DL
secondary dysgenetic glaucoma associated with neural crest cell migration anomaly	0.9799	DL
hereditary thrombocytopenia with normal platelets	0.9799	DL
rheumatoid arthritis	0.9799	DL
transient neonatal thrombocytopenia	0.9796	DL
dense granule disease	0.9784	DL
roseolovirus infectious disease	0.9781	DL
drug-induced osteoporosis	0.9777	DL
pulmonary hypertension	0.9775	DL
thrombotic disease	0.9768	DL
Leydig cell hypoplasia due to LH resistance	0.9764	DL
kyphoscoliotic heart disease	0.9763	DL
neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter	0.9762	DL
brachydactyly-syndactyly syndrome	0.9760	DL
46,XY disorder of sex development due to impaired androgen production	0.9753	DL
antithrombin deficiency type 2	0.9745	DL
dermatofibrosarcoma protuberans	0.9743	DL
factor 5 excess with spontaneous thrombosis	0.9731	DL
heparin cofactor 2 deficiency	0.9716	DL
hyperthyroidism	0.9704	DL
colobomatous microphthalmia-rhizomelic dysplasia syndrome	0.9700	DL

External Links

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