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: C1848030
Disease: Hypotonia-Cystinuria Syndrome
Hypotonia-Cystinuria Syndrome 		6 0 6 0.27 0 0
CUI: C0268643
Disease: Cystinuria type 1
Cystinuria type 1 		4 7 4 0.18 3 3.4E-02
CUI: C4304537
Disease: 2p21 microdeletion syndrome
2p21 microdeletion syndrome 		4 0 4 0.18 0 0
CUI: C4755274
Disease: Atypical hypotonia cystinuria syndrome
Atypical hypotonia cystinuria syndrome 		4 0 4 0.18 0 0
CUI: C0268646
Disease: Isolated cystinuria
Isolated cystinuria 		3 0 3 0.14 0 0
CUI: C4025602
Disease: Ornithinuria
Ornithinuria 		3 0 3 0.14 0 0
CUI: C4025635
Disease: Argininuria
Argininuria 		3 0 3 0.14 0 0
CUI: C0024788
Disease: Marburg Virus Disease
Marburg Virus Disease 		4 0 3 0.13 0 0
CUI: C4021733
Disease: Hyperlysinuria
Hyperlysinuria 		4 0 3 0.13 0 0
CUI: C0268647
Disease: Lysinuric Protein Intolerance
Lysinuric Protein Intolerance 		21 0 4 0.10 0 0
CUI: C2751582
Disease: Mitochondrial respiratory chain defects
Mitochondrial respiratory chain defects 		21 0 4 0.10 0 0
CUI: C0948859
Disease: Oxalate crystalluria
Oxalate crystalluria 		2 0 2 9.1E-02 0 0
CUI: C1857389
Disease: Cystinuria, Type B
Cystinuria, Type B 		2 0 2 9.1E-02 0 0
CUI: C3698119
Disease: Inherited aminoaciduria
Inherited aminoaciduria 		2 0 2 9.1E-02 0 0
CUI: C4479088
Disease: MYASTHENIC SYNDROME, CONGENITAL, 22
MYASTHENIC SYNDROME, CONGENITAL, 22 		2 0 2 9.1E-02 0 0
CUI: C4749458
Disease: 2p21 microdeletion syndrome without cystinuria
2p21 microdeletion syndrome without cystinuria 		2 0 2 9.1E-02 0 0
CUI: C1842681
Disease: Hypoplastic helices
Hypoplastic helices 		4 0 2 8.3E-02 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome 		31 0 4 8.2E-02 0 0
CUI: C0085547
Disease: Phenylketonuria, Maternal
Phenylketonuria, Maternal 		6 0 2 7.7E-02 0 0
CUI: C1833213
Disease: Hyperferritinemia, hereditary, with congenital cataracts
Hyperferritinemia, hereditary, with congenital cataracts 		10 0 2 6.7E-02 0 0
CUI: C0343239
Disease: Benign congenital hypotonia
Benign congenital hypotonia 		11 0 2 6.5E-02 0 0
CUI: C0853068
Disease: Decreased glomerular filtration rate
Decreased glomerular filtration rate 		11 0 2 6.5E-02 0 0
CUI: C0346991
Disease: Secondary malignant neoplasm of omentum
Secondary malignant neoplasm of omentum 		14 0 2 5.9E-02 0 0
CUI: C0007930
Disease: Chagas Cardiomyopathy
Chagas Cardiomyopathy 		37 0 3 5.4E-02 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 2 5.0E-02 0 0