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: C0472387
Disease: Vasogenic Cerebral Edema
Vasogenic Cerebral Edema 		8 0 8 0.31 0 0
CUI: C0472388
Disease: Cytotoxic Cerebral Edema
Cytotoxic Cerebral Edema 		8 0 8 0.31 0 0
CUI: C0750969
Disease: Vasogenic Brain Edema
Vasogenic Brain Edema 		8 0 8 0.31 0 0
CUI: C0750970
Disease: Cytotoxic Brain Edema
Cytotoxic Brain Edema 		8 0 8 0.31 0 0
CUI: C1527311
Disease: Brain Edema
Brain Edema 		30 0 8 0.17 0 0
CUI: C1839541
Disease: Episodic ammonia intoxication
Episodic ammonia intoxication 		4 0 4 0.15 0 0
CUI: C1839531
Disease: Protein avoidance
Protein avoidance 		5 0 4 0.15 0 0
CUI: C0002064
Disease: Alkalosis, Respiratory
Alkalosis, Respiratory 		6 0 4 0.14 0 0
CUI: C0009421
Disease: Comatose
Comatose 		78 0 13 0.14 0 0
CUI: C0154246
Disease: Urea Cycle Disorders, Inborn
Urea Cycle Disorders, Inborn 		14 0 4 0.11 0 0
CUI: C4024697
Disease: Elevated plasma branched chain amino acids
Elevated plasma branched chain amino acids 		4 0 3 0.11 0 0
CUI: C4025095
Disease: Hypoargininemia
Hypoargininemia 		4 0 3 0.11 0 0
CUI: C0268568
Disease: Classic Maple Syrup Urine Disease
Classic Maple Syrup Urine Disease 		5 0 3 0.11 0 0
CUI: C0268569
Disease: Intermittent Maple Syrup Urine Disease
Intermittent Maple Syrup Urine Disease 		5 0 3 0.11 0 0
CUI: C0751285
Disease: Maple Syrup Urine Disease, Thiamine Responsive
Maple Syrup Urine Disease, Thiamine Responsive 		5 0 3 0.11 0 0
CUI: C1621920
Disease: Intermediate Maple Syrup Urine Disease
Intermediate Maple Syrup Urine Disease 		5 0 3 0.11 0 0
CUI: C1839533
Disease: Hyperglutaminemia
Hyperglutaminemia 		5 0 3 0.11 0 0
CUI: C0175683
Disease: Citrullinemia
Citrullinemia 		7 0 3 1.0E-01 0 0
CUI: C4703632
Disease: Increased level of hippuric acid in urine
Increased level of hippuric acid in urine 		7 0 3 1.0E-01 0 0
CUI: C1855020
Disease: Acute necrotizing encephalopathy
Acute necrotizing encephalopathy 		8 0 3 9.7E-02 0 0
CUI: C0268548
Disease: Hyperargininemia
Hyperargininemia 		11 0 3 8.8E-02 0 0
CUI: C4023117
Disease: Decreased plasma total carnitine
Decreased plasma total carnitine 		2 0 2 7.7E-02 0 0
CUI: C4082171
Disease: Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency
Hyperammonemia Due to Carbamoyl Phosphate Synthetase 1 Deficiency 		2 0 2 7.7E-02 0 0
CUI: C0220994
Disease: Hyperammonemia
Hyperammonemia 		102 0 9 7.6E-02 0 0
CUI: C1306587
Disease: Acute encephalopathy
Acute encephalopathy 		31 0 4 7.5E-02 0 0