Galsulfase

DrugBank ID: DB01279

Summary

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

Predictions

Indication	Score	Source
ptosis-strabismus-ectopic pupils syndrome	0.9789	DL
camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye	0.9787	DL
congenital Horner syndrome (disease)	0.9784	DL
ptosis-vocal cord paralysis syndrome	0.9783	DL
ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome	0.9767	DL
jaw-winking syndrome	0.9765	DL
congenital entropion	0.9764	DL
epiblepharon	0.9755	DL
congenital ectropion	0.9748	DL
mucopolysaccharidosis	0.9693	KG+DL
Scheie syndrome	0.9479	DL
Steel syndrome	0.9388	DL
inborn disorder of lysosomal amino acid transport	0.9243	DL
proximal myopathy with extrapyramidal signs	0.9131	DL
Hurler syndrome	0.9023	DL
Charcot-Marie-Tooth disease	0.9005	DL
Sanfilippo syndrome	0.8867	DL
lysosomal storage disease with skeletal involvement	0.8799	DL
alpha-mannosidosis	0.8723	DL
skeletal muscle disease	0.8619	DL
hypophosphatasia	0.8590	DL
inclusion myopathy	0.8421	DL
phosphoribosylpyrophosphate synthetase superactivity	0.7904	DL
ocular cystinosis	0.7873	DL
esophageal varices with bleeding	0.7789	DL
esophageal varices without bleeding	0.7789	DL
myoclonic epilepsy, juvenile, susceptibility to	0.7614	DL
familial encephalopathy with neuroserpin inclusion bodies	0.7539	DL
infantile neuronal ceroid lipofuscinosis	0.7378	DL
lysosomal disease with hypertrophic cardiomyopathy	0.7327	DL
syndromic neurometabolic disease with X-linked intellectual disability	0.7305	DL
growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant	0.7301	DL
eyelids malposition disorder	0.7293	DL
Tay-Sachs disease	0.7140	DL
adolescent/adult-onset epilepsy syndrome	0.7136	DL
adolescence-adult electroclinical syndrome	0.6972	DL
adult Krabbe disease	0.6913	DL
mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies	0.6801	DL
reticular dysgenesis	0.6691	DL
Oguchi disease	0.6655	DL
optic atrophy 10 with or without ataxia, intellectual disability, and seizures	0.6654	DL
TBCK-related intellectual disability syndrome	0.6622	DL
osteosclerotic metaphyseal dysplasia	0.6621	DL
mucolipidosis type III gamma	0.6596	DL
hereditary xanthinuria	0.6592	DL
lathosterolosis	0.6558	DL
trichohepatoenteric syndrome	0.6516	DL
familial generalized lentiginosis	0.6502	DL
hereditary myopathy with lactic acidosis due to ISCU deficiency	0.6496	DL
arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome	0.6444	DL

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