Penicillamine

DrugBank ID: DB00859

Summary

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

Predictions

Indication	Score	Source
megaloblastic anemia (disease)	0.9802	DL
galactosemia	0.9643	DL
glycogen storage disease	0.9428	DL
tricarboxylic acid cycle disorder	0.9346	DL
disease of transporter activity	0.9302	DL
neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter	0.9301	DL
glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form	0.9288	DL
glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form	0.9288	DL
adult polyglucosan body disease	0.9249	DL
granulomatous disease, chronic, X-linked	0.9248	DL
hereditary hemochromatosis	0.9237	DL
autosomal recessive severe congenital neutropenia due to G6PC3 deficiency	0.9231	DL
pyruvate metabolism disorder	0.9154	DL
anemia, nonspherocytic hemolytic, due to G6PD deficiency	0.9026	DL
inborn disorder of fatty acid oxidation and ketone body metabolism	0.9022	DL
disorder of mineral absorption and transport	0.9022	DL
hemolytic anemia due to diphosphoglycerate mutase deficiency	0.9002	DL
HIV infectious disease	0.8994	DL
primary immunodeficiency syndrome due to p14 deficiency	0.8953	DL
Wilson disease	0.8941	DL
glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form	0.8938	DL
glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form	0.8938	DL
glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form	0.8938	DL
glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form	0.8938	DL
glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form	0.8938	DL
glycogen storage disease due to glucose-6-phosphatase deficiency	0.8852	DL
G6PD deficiency	0.8841	DL
obsolete rare hereditary hemochromatosis	0.8810	DL
oculocerebral hypopigmentation syndrome, Cross type	0.8780	DL
Griscelli syndrome	0.8775	DL
cold agglutinin disease	0.8760	DL
Hermansky-Pudlak syndrome with pulmonary fibrosis	0.8713	DL
iron metabolism disease	0.8709	DL
ermine phenotype	0.8705	DL
Hermansky-Pudlak syndrome without pulmonary fibrosis	0.8698	DL
primary CD59 deficiency	0.8694	DL
piebaldism	0.8684	DL
ocular albinism with sensorineural deafness	0.8672	DL
paraplegia	0.8652	DL
albinism	0.8633	DL
glycogen storage disease due to muscle and heart glycogen synthase deficiency	0.8629	DL
classic galactosemia	0.8545	DL
feline acquired immunodeficiency syndrome	0.8543	DL
simian immunodeficiency virus infection	0.8543	DL
galactokinase deficiency	0.8528	DL
ocular albinism (disease)	0.8516	DL
minimal pigment oculocutaneous albinism type 1	0.8511	DL
temperature-sensitive oculocutaneous albinism type 1	0.8505	DL
primary hyperoxaluria	0.8492	DL
hemochromatosis	0.8473	DL

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