Taliglucerase alfa

DrugBank ID: DB08876

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	1
DL Only	49
KG Only	0

Predictions

Indication	Score	Source
Hurler syndrome	0.9952	DL
Gaucher disease	0.9940	KG+DL
Scheie syndrome	0.9929	DL
benign neoplasm of adrenal gland	0.9928	DL
autosomal ichthyosis syndrome with fatal disease course	0.9924	DL
cholesteryl ester storage disease	0.9912	DL
lysosomal storage disease with skeletal involvement	0.9894	DL
Wolman disease with hypolipoproteinemia and acanthocytosis	0.9893	DL
Wolman disease	0.9878	DL
proximal myopathy with extrapyramidal signs	0.9854	DL
growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant	0.9849	DL
Tay-Sachs disease	0.9841	DL
familial apolipoprotein C-II deficiency	0.9837	DL
adult Krabbe disease	0.9836	DL
encephalopathy due to prosaposin deficiency	0.9830	DL
Krabbe disease	0.9815	DL
X-linked lymphoproliferative disease due to SH2D1A deficiency	0.9813	DL
Cushing disease due to pituitary adenoma	0.9809	DL
lysosomal acid lipase deficiency	0.9798	DL
metachromatic leukodystrophy	0.9797	DL
skeletal muscle disease	0.9794	DL
Steel syndrome	0.9782	DL
inclusion myopathy	0.9770	DL
alpha-mannosidosis	0.9759	DL
A20 haploinsufficiency	0.9752	DL
immune dysregulation with inflammatory bowel disease	0.9732	DL
syndromic neurometabolic disease with X-linked intellectual disability	0.9730	DL
recessive X-linked ichthyosis	0.9728	DL
lysosomal disease with hypertrophic cardiomyopathy	0.9728	DL
infantile neuronal ceroid lipofuscinosis	0.9711	DL
eyelids malposition disorder	0.9706	DL
free sialic acid storage disease	0.9701	DL
Sanfilippo syndrome	0.9700	DL
Gaucher disease perinatal lethal	0.9693	DL
gangliosidosis	0.9684	DL
familial encephalopathy with neuroserpin inclusion bodies	0.9666	DL
ptosis-vocal cord paralysis syndrome	0.9649	DL
congenital Horner syndrome (disease)	0.9644	DL
camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye	0.9641	DL
ptosis-strabismus-ectopic pupils syndrome	0.9632	DL
Fabry disease	0.9626	DL
lipase deficiency, combined	0.9623	DL
ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome	0.9620	DL
hypophosphatasia	0.9620	DL
myoclonic epilepsy, juvenile, susceptibility to	0.9619	DL
familial restrictive cardiomyopathy	0.9618	DL
adolescent/adult-onset epilepsy syndrome	0.9617	DL
cholesterol metabolism disease	0.9612	DL
neuronal ceroid lipofuscinosis 8 northern epilepsy variant	0.9608	DL
jaw-winking syndrome	0.9603	DL

External Links

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