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: C3698119
Disease: Inherited aminoaciduria
Inherited aminoaciduria 		2 0 2 1.00 0 0
CUI: C4025602
Disease: Ornithinuria
Ornithinuria 		3 0 2 0.67 0 0
CUI: C4025635
Disease: Argininuria
Argininuria 		3 0 2 0.67 0 0
CUI: C0268643
Disease: Cystinuria type 1
Cystinuria type 1 		4 0 2 0.50 0 0
CUI: C0268645
Disease: Cystinuria, type 3
Cystinuria, type 3 		1 0 1 0.50 0 0
CUI: C1857388
Disease: Cystinuria, Type A
Cystinuria, Type A 		1 0 1 0.50 0 0
CUI: C4021733
Disease: Hyperlysinuria
Hyperlysinuria 		4 0 2 0.50 0 0
CUI: C4479088
Disease: MYASTHENIC SYNDROME, CONGENITAL, 22
MYASTHENIC SYNDROME, CONGENITAL, 22 		2 0 1 0.33 0 0
CUI: C0268646
Disease: Isolated cystinuria
Isolated cystinuria 		3 0 1 0.25 0 0
CUI: C0024788
Disease: Marburg Virus Disease
Marburg Virus Disease 		4 0 1 0.20 0 0
CUI: C4304537
Disease: 2p21 microdeletion syndrome
2p21 microdeletion syndrome 		4 0 1 0.20 0 0
CUI: C4755274
Disease: Atypical hypotonia cystinuria syndrome
Atypical hypotonia cystinuria syndrome 		4 0 1 0.20 0 0
CUI: C1848030
Disease: Hypotonia-Cystinuria Syndrome
Hypotonia-Cystinuria Syndrome 		6 0 1 0.14 0 0
CUI: C1866956
Disease: Aortic root dilation
Aortic root dilation 		9 0 1 1.0E-01 0 0
CUI: C0010691
Disease: Cystinuria
Cystinuria 		22 0 2 9.1E-02 0 0
CUI: C0343239
Disease: Benign congenital hypotonia
Benign congenital hypotonia 		11 0 1 8.3E-02 0 0
CUI: C1850889
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B 		19 0 1 5.0E-02 0 0
CUI: C0268647
Disease: Lysinuric Protein Intolerance
Lysinuric Protein Intolerance 		21 0 1 4.5E-02 0 0
CUI: C2751582
Disease: Mitochondrial respiratory chain defects
Mitochondrial respiratory chain defects 		21 0 1 4.5E-02 0 0
CUI: C0238506
Disease: Congenital posterior urethral valves
Congenital posterior urethral valves 		26 0 1 3.7E-02 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		31 0 1 3.1E-02 0 0
CUI: C0007930
Disease: Chagas Cardiomyopathy
Chagas Cardiomyopathy 		37 0 1 2.6E-02 0 0
CUI: C0027707
Disease: Nephritis, Interstitial
Nephritis, Interstitial 		79 0 2 2.5E-02 0 0
CUI: C0497552
Disease: Congenital neurologic anomalies
Congenital neurologic anomalies 		84 0 2 2.4E-02 0 0
CUI: C0041349
Disease: Nephritis, Tubulointerstitial
Nephritis, Tubulointerstitial 		92 0 2 2.2E-02 0 0