Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C4025603
Disease: Glutaric acidemia
Glutaric acidemia 		5 0 5 0.62 0 0
CUI: C0546389
Disease: Hepatic periportal necrosis
Hepatic periportal necrosis 		3 0 3 0.38 0 0
CUI: C1856401
Disease: Glutaric Aciduria IIA
Glutaric Aciduria IIA 		3 0 3 0.38 0 0
CUI: C1856403
Disease: Glutaric Aciduria IIB
Glutaric Aciduria IIB 		3 0 3 0.38 0 0
CUI: C1856405
Disease: Glutaric Aciduria IIC
Glutaric Aciduria IIC 		3 0 3 0.38 0 0
CUI: C4025586
Disease: Electron transfer flavoprotein-ubiquinone oxidoreductase defect
Electron transfer flavoprotein-ubiquinone oxidoreductase defect 		3 0 3 0.38 0 0
CUI: C1853136
Disease: Neutral Lipid Storage Disease with Myopathy
Neutral Lipid Storage Disease with Myopathy 		6 0 3 0.27 0 0
CUI: C1865353
Disease: Ethylmalonic aciduria
Ethylmalonic aciduria 		6 0 3 0.27 0 0
CUI: C3151952
Disease: 3-Methylglutaric aciduria
3-Methylglutaric aciduria 		3 0 2 0.22 0 0
CUI: C3152055
Disease: D-2-HYDROXYGLUTARIC ACIDURIA 1
D-2-HYDROXYGLUTARIC ACIDURIA 1 		4 0 2 0.20 0 0
CUI: C1847868
Disease: Generalized aminoaciduria
Generalized aminoaciduria 		11 0 3 0.19 0 0
CUI: C0020617
Disease: Hypoglycemic coma
Hypoglycemic coma 		19 0 4 0.17 0 0
CUI: C0369183
Disease: Erythrocyte Mean Corpuscular Hemoglobin Test
Erythrocyte Mean Corpuscular Hemoglobin Test 		13 0 3 0.17 0 0
CUI: C1969144
Disease: Renal cortical cysts
Renal cortical cysts 		14 0 3 0.16 0 0
CUI: C0271902
Disease: Microcytic normochromic anemia
Microcytic normochromic anemia 		1 0 1 0.12 0 0
CUI: C1533587
Disease: Hydroxymethylglutaric aciduria
Hydroxymethylglutaric aciduria 		1 0 1 0.12 0 0
CUI: C1837257
Disease: Lipid accumulation in hepatocytes
Lipid accumulation in hepatocytes 		1 0 1 0.12 0 0
CUI: C3278154
Disease: GLUTARIC ACIDEMIA IIA
GLUTARIC ACIDEMIA IIA 		1 0 1 0.12 0 0
CUI: C3278155
Disease: GLUTARIC ACIDEMIA IIB
GLUTARIC ACIDEMIA IIB 		1 0 1 0.12 0 0
CUI: C3278156
Disease: GLUTARIC ACIDEMIA IIC
GLUTARIC ACIDEMIA IIC 		1 0 1 0.12 0 0
CUI: C4016438
Disease: GLUTARIC ACIDEMIA IIC, LATE-ONSET
GLUTARIC ACIDEMIA IIC, LATE-ONSET 		1 0 1 0.12 0 0
CUI: C4023058
Disease: Abnormality of acetylcarnitine metabolism
Abnormality of acetylcarnitine metabolism 		1 0 1 0.12 0 0
CUI: C4024972
Disease: Symmetrical progressive peripheral demyelination
Symmetrical progressive peripheral demyelination 		1 0 1 0.12 0 0
CUI: C4039473
Disease: 3-methylglutaconic aciduria type 5
3-methylglutaconic aciduria type 5 		1 0 1 0.12 0 0
CUI: C4703617
Disease: Increased level of 3-hydroxy-3-methylglutaric acid in urine
Increased level of 3-hydroxy-3-methylglutaric acid in urine 		1 0 1 0.12 0 0