Pioglitazone

DrugBank ID: DB01132

Summary

Metric	Value
Total Predictions	50
KG+DL (Dual Validated)	2
DL Only	48
KG Only	0

Predictions

Indication	Score	Source
opsismodysplasia	0.9959	DL
diabetes mellitus (disease)	0.9956	KG+DL
classic stiff person syndrome	0.9950	DL
focal stiff limb syndrome	0.9950	DL
thiamine-responsive dysfunction syndrome	0.9948	DL
drug-induced localized lipodystrophy	0.9930	DL
centrifugal lipodystrophy	0.9926	DL
pressure-induced localized lipoatrophy	0.9924	DL
idiopathic localized lipodystrophy	0.9919	DL
pancreatic agenesis	0.9918	DL
autoimmune oophoritis	0.9806	DL
type 1 diabetes mellitus	0.9801	DL
homozygous familial hypercholesterolemia	0.8535	DL
diabetes mellitus, insulin-dependent, X-linked, susceptibility to	0.7779	DL
permanent neonatal diabetes mellitus	0.6918	DL
type 2 diabetes mellitus	0.6547	KG+DL
cholangiocarcinoma, susceptibility to	0.6371	DL
hemoglobin C-beta-thalassemia syndrome	0.6018	DL
obsolete breast fibroadenosis	0.5991	DL
mitral valve prolapse, myxomatous	0.5991	DL
atrial flutter (disease)	0.5977	DL
hypercarotenemia and vitamin A deficiency, autosomal recessive	0.5977	DL
congenital temporomandibular joint ankylosis	0.5950	DL
obsolete functional visual loss	0.5898	DL
woolly hair, autosomal recessive 3	0.5871	DL
pancreas, dorsal, agenesis of	0.5789	DL
familial chronic myelocytic leukemia-like syndrome	0.5764	DL
fetal growth restriction	0.5724	DL
polydipsia	0.5712	DL
trichoepitheliomas, multiple desmoplastic	0.5652	DL
anuria	0.5636	DL
radiation proctitis	0.5636	DL
ovarian fibroma (disease)	0.5619	DL
lymphatic malformation 8	0.5605	DL
prostate cancer, hereditary, X-linked	0.5579	DL
guttate psoriasis	0.5572	DL
conduct disorder	0.5568	DL
avascular necrosis	0.5561	DL
WT limb-blood syndrome	0.5557	DL
giant neutrophil leukocytes	0.5549	DL
sudden arrhythmia death syndrome	0.5546	DL
milia, multiple eruptive	0.5539	DL
sunburn	0.5534	DL
nonarteritic anterior ischemic optic neuropathy, susceptibility to	0.5526	DL
obsolete pathologic fracture	0.5523	DL
lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis	0.5510	DL
Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin	0.5505	DL
hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome	0.5497	DL
obsolete superimposed infection	0.5490	DL
obsolete left bundle branch block	0.5464	DL

External Links

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