Aluminum oxide

DrugBank ID: DB11342

Summary

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

Predictions

Indication	Score	Source
rheumatoid arthritis	0.9998	DL
brachydactyly-syndactyly syndrome	0.9996	DL
colobomatous microphthalmia-rhizomelic dysplasia syndrome	0.9996	DL
heparin cofactor 2 deficiency	0.9990	DL
hemoglobinopathy	0.9990	DL
factor 5 excess with spontaneous thrombosis	0.9990	DL
antithrombin deficiency type 2	0.9989	DL
thrombotic disease	0.9987	DL
beta-thalassemia with other manifestations	0.9985	DL
hemolytic anemia due to glucophosphate isomerase deficiency	0.9984	DL
partial deletion of the short arm of chromosome 16	0.9983	DL
thrombophilia	0.9983	DL
pyruvate kinase deficiency of red cells	0.9982	DL
pyropoikilocytosis, hereditary	0.9980	DL
myocardial infarction (disease)	0.9979	DL
amyotrophic lateral sclerosis	0.9979	DL
gout	0.9976	DL
Mills syndrome	0.9969	DL
amyotrophic lateral sclerosis, susceptibility to	0.9969	DL
amyotrohpic lateral sclerosis type 22	0.9968	DL
plasma cell myeloma	0.9966	DL
heart disease	0.9966	DL
lower motor neuron syndrome with late-adult onset	0.9965	DL
bilateral parasagittal parieto-occipital polymicrogyria	0.9965	DL
vein disease	0.9964	DL
sickle cell anemia	0.9964	DL
myeloid leukemia	0.9963	DL
axial spondylometaphyseal dysplasia	0.9962	DL
monomelic amyotrophy	0.9961	DL
female breast carcinoma	0.9960	DL
lethal arthrogryposis-anterior horn cell disease syndrome	0.9959	DL
autosomal dominant mitochondrial myopathy with exercise intolerance	0.9959	DL
hereditary persistence of fetal hemoglobin-sickle cell disease syndrome	0.9957	DL
sickle cell-beta-thalassemia disease syndrome	0.9957	DL
sickle cell-hemoglobin E disease syndrome	0.9957	DL
sickle cell-hemoglobin c disease syndrome	0.9957	DL
sickle cell-hemoglobin d disease syndrome	0.9957	DL
trichomegaly-retina pigmentary degeneration-dwarfism syndrome	0.9957	DL
HIV infectious disease	0.9957	DL
interventricular septum aneurysm	0.9957	DL
arteriosclerosis disorder	0.9956	DL
Laubry-Pezzi syndrome	0.9955	DL
coronary thrombosis	0.9955	DL
Jeune syndrome situs inversus	0.9954	DL
Pierre Robin syndrome associated with a chromosomal anomaly	0.9954	DL
genetic syndromic Pierre Robin syndrome	0.9954	DL
partial deletion of the long arm of chromosome 22	0.9954	DL
partial deletion of the long arm of chromosome 7	0.9954	DL
pulmonary valve disease	0.9953	DL
mitral valve disease	0.9953	DL

External Links

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