Protamine sulfate

DrugBank ID: DB09141

Summary

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

Predictions

Indication	Score	Source
CDKL5 disorder	0.5000	DL
ECHS1-related paroxysmal dyskinesia	0.5000	DL
EEC syndrome	0.5000	DL
FOXG1 disorder	0.5000	DL
MED12-related intellectual disability syndrome	0.5000	DL
PRPS1 deficiency disorder	0.5000	DL
Pericytoma with t(7;12)	0.5000	DL
Rowley-Rosenberg syndrome	0.5000	DL
TH-deficient infantile parkinsonism and motor delay	0.5000	DL
acetazolamide-responsive hereditary episodic ataxia	0.5000	DL
adolescent/adult onset autosomal dominant epilepsy with auditory features	0.5000	DL
adolescent/adult-onset epilepsy syndrome	0.5000	DL
adult-onset segmental dystonia	0.5000	DL
alpha-gal syndrome	0.5000	DL
anaphylaxis	0.5000	DL
antibody mediated epilepsy	0.5000	DL
atypical childhood epilepsy with centrotemporal spikes	0.5000	DL
autoimmune retinopathy	0.5000	DL
cerebral folate deficiency	0.5000	DL
complex neurodevelopmental disorder	0.5000	DL
ectodermal dysplasia syndrome	0.5000	DL
epilepsy of infancy with migrating focal seizures	0.5000	DL
exercise-induced anaphylaxis	0.5000	DL
febrile seizures plus, genetic epilepsy with febrile seizures plus	0.5000	DL
food protein-induced allergic proctocolitis	0.5000	DL
food protein-induced enterocolitis syndrome	0.5000	DL
food-dependent exercise-induced anaphylaxis	0.5000	DL
hypereosinophilia of undetermined significance	0.5000	DL
hypervalinemia and hyperleucine-isoleucinemia	0.5000	DL
idiopathic anaphylaxis	0.5000	DL
idiopathic mast cell activation syndrome	0.5000	DL
immune epilepsy	0.5000	DL
mast cell activation syndrome	0.5000	DL
metabolic epilepsy	0.5000	DL
mixed mineral dust pneumoconiosis	0.5000	DL
myoclonic encephalopathy in non-progressive disorder	0.5000	DL
neonatal/infantile epilepsy syndrome	0.5000	DL
paratenonitis	0.5000	DL
paratenonitis with tendinosis	0.5000	DL
photosensitive occipital lobe epilepsy	0.5000	DL
primary mast cell activation syndrome	0.5000	DL
rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction	0.5000	DL
saccharopinuria	0.5000	DL
secondary mast cell activation syndrome	0.5000	DL
self-limited familial and non-familial neonatal/infantile seizures	0.5000	DL
structural epilepsy	0.5000	DL
tendinopathy	0.5000	DL
tendinosis	0.5000	DL
tyrosine hydroxylase deficiency	0.5000	DL
variable age onset epilepsy	0.5000	DL

External Links

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