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: C4703634
Disease: Increased level of L-glutamic acid in blood
Increased level of L-glutamic acid in blood 		1 0 1 1.00 0 0
CUI: C1850413
Disease: Reye syndrome-like episodes
Reye syndrome-like episodes 		4 0 1 0.25 0 0
CUI: C1839533
Disease: Hyperglutaminemia
Hyperglutaminemia 		5 0 1 0.20 0 0
CUI: C1859506
Disease: Acute hyperammonemia
Acute hyperammonemia 		5 0 1 0.20 0 0
CUI: C0041657
Disease: Unconscious State
Unconscious State 		13 0 1 7.7E-02 0 0
CUI: C0154246
Disease: Urea Cycle Disorders, Inborn
Urea Cycle Disorders, Inborn 		14 0 1 7.1E-02 0 0
CUI: C0021290
Disease: Neonatal disorder
Neonatal disorder 		15 0 1 6.7E-02 0 0
CUI: C0268579
Disease: Propionic acidemia
Propionic acidemia 		17 0 1 5.9E-02 0 0
CUI: C0268647
Disease: Lysinuric Protein Intolerance
Lysinuric Protein Intolerance 		21 0 1 4.8E-02 0 0
CUI: C0276096
Disease: Mastitis-metritis-agalactia syndrome
Mastitis-metritis-agalactia syndrome 		23 0 1 4.3E-02 0 0
CUI: C0013144
Disease: Drowsiness
Drowsiness 		31 0 1 3.2E-02 0 0
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes 		31 0 1 3.2E-02 0 0
CUI: C0268630
Disease: Hyper-beta-alaninemia
Hyper-beta-alaninemia 		33 0 1 3.0E-02 0 0
CUI: C0013528
Disease: Echolalia
Echolalia 		39 0 1 2.6E-02 0 0
CUI: C0268583
Disease: Methylmalonic acidemia
Methylmalonic acidemia 		44 0 1 2.3E-02 0 0
CUI: C0030486
Disease: Paraplegia
Paraplegia 		59 0 1 1.7E-02 0 0
CUI: C0232462
Disease: Decrease in appetite
Decrease in appetite 		62 0 1 1.6E-02 0 0
CUI: C1963099
Disease: Myelodysplasia, CTCAE
Myelodysplasia, CTCAE 		68 0 1 1.5E-02 0 0
CUI: C0009676
Disease: Confusion
Confusion 		75 0 1 1.3E-02 0 0
CUI: C0009421
Disease: Comatose
Comatose 		78 0 1 1.3E-02 0 0
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias 		83 0 1 1.2E-02 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0 		87 0 1 1.1E-02 0 0
CUI: C2830004
Disease: Somnolence
Somnolence 		87 0 1 1.1E-02 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0 		87 0 1 1.1E-02 0 0
CUI: C0220994
Disease: Hyperammonemia
Hyperammonemia 		102 0 1 9.8E-03 0 0