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: C0268514
Disease: Urocanase deficiency
Urocanase deficiency 		1 0 1 7.1E-02 0 0
CUI: C0598675
Disease: inborn aminoaciduria
inborn aminoaciduria 		1 0 1 7.1E-02 0 0
CUI: C0856208
Disease: Increased serum zinc
Increased serum zinc 		1 0 1 7.1E-02 0 0
CUI: C3809845
Disease: EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE, 2 		1 0 1 7.1E-02 0 0
CUI: C0741270
Disease: Intermittent ataxia
Intermittent ataxia 		2 0 1 6.7E-02 0 0
CUI: C1866294
Disease: EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 		2 0 1 6.7E-02 0 0
CUI: C4023102
Disease: Elevated plasma citrulline
Elevated plasma citrulline 		2 0 1 6.7E-02 0 0
CUI: C4025602
Disease: Ornithinuria
Ornithinuria 		3 0 1 6.2E-02 0 0
CUI: C4025635
Disease: Argininuria
Argininuria 		3 0 1 6.2E-02 0 0
CUI: C0267839
Disease: Hepatic amyloidosis
Hepatic amyloidosis 		4 0 1 5.9E-02 0 0
CUI: C0268528
Disease: Hyperprolinemia
Hyperprolinemia 		4 0 1 5.9E-02 0 0
CUI: C0268643
Disease: Cystinuria type 1
Cystinuria type 1 		4 0 1 5.9E-02 0 0
CUI: C1266088
Disease: Adenocarcinoma with neuroendocrine differentiation
Adenocarcinoma with neuroendocrine differentiation 		4 0 1 5.9E-02 0 0
CUI: C4021733
Disease: Hyperlysinuria
Hyperlysinuria 		4 0 1 5.9E-02 0 0
CUI: C4302857
Disease: Malignancy-associated membranous nephropathy
Malignancy-associated membranous nephropathy 		4 0 1 5.9E-02 0 0
CUI: C0002989
Disease: Epithelioid hemangioma of skin
Epithelioid hemangioma of skin 		5 0 1 5.6E-02 0 0
CUI: C0151701
Disease: Pulmonary hemorrhage
Pulmonary hemorrhage 		5 0 1 5.6E-02 0 0
CUI: C0475713
Disease: Perinatal pulmonary hemorrhage
Perinatal pulmonary hemorrhage 		5 0 1 5.6E-02 0 0
CUI: C1839533
Disease: Hyperglutaminemia
Hyperglutaminemia 		5 0 1 5.6E-02 0 0
CUI: C0017614
Disease: Glaucoma, Suspect
Glaucoma, Suspect 		6 0 1 5.3E-02 0 0
CUI: C0268128
Disease: Orotic aciduria
Orotic aciduria 		6 0 1 5.3E-02 0 0
CUI: C3665983
Disease: Oral aversion
Oral aversion 		7 0 1 5.0E-02 0 0
CUI: C0149696
Disease: Food intolerance (disorder)
Food intolerance (disorder) 		8 0 1 4.8E-02 0 0
CUI: C0238577
Disease: Abdominal wall defect
Abdominal wall defect 		8 0 1 4.8E-02 0 0
CUI: C1536168
Disease: Chronic pelvic pain syndrome
Chronic pelvic pain syndrome 		8 0 1 4.8E-02 0 0