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: C0012714
Disease: Disorder of copper metabolism
Disorder of copper metabolism 		5 0 3 0.21 0 0
CUI: C0268070
Disease: Hypocupremia
Hypocupremia 		23 2 6 0.21 2 0.40
CUI: C0152457
Disease: Kayser-Fleischer ring
Kayser-Fleischer ring 		2 0 2 0.17 0 0
CUI: C1845359
Disease: Spinal Muscular Atrophy, Distal, X-Linked 3
Spinal Muscular Atrophy, Distal, X-Linked 3 		2 0 2 0.17 0 0
CUI: C1836330
Disease: ERYTHROKERATODERMIA VARIABILIS 3 (disorder)
ERYTHROKERATODERMIA VARIABILIS 3 (disorder) 		3 0 2 0.15 0 0
CUI: C0022716
Disease: Menkes Kinky Hair Syndrome
Menkes Kinky Hair Syndrome 		20 99 4 0.14 1 9.7E-03
CUI: C4022946
Disease: Abnormal glycosylation
Abnormal glycosylation 		6 0 2 0.12 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 2 0.11 0 0
CUI: C0151731
Disease: Hepatic infarction
Hepatic infarction 		1 0 1 8.3E-02 0 0
CUI: C0302332
Disease: Poisoning syndrome
Poisoning syndrome 		14 0 2 8.3E-02 0 0
CUI: C0474679
Disease: Serum ceruloplasmin measurement
Serum ceruloplasmin measurement 		1 0 1 8.3E-02 0 0
CUI: C0840564
Disease: Rupture of bladder
Rupture of bladder 		1 0 1 8.3E-02 0 0
CUI: C1303076
Disease: Tortuous carotid artery
Tortuous carotid artery 		1 0 1 8.3E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 8.3E-02 0 0
CUI: C1843852
Disease: SPINOCEREBELLAR ATAXIA WITH EPILEPSY
SPINOCEREBELLAR ATAXIA WITH EPILEPSY 		1 0 1 8.3E-02 0 0
CUI: C1848456
Disease: Atypical or prolonged hepatitis
Atypical or prolonged hepatitis 		1 0 1 8.3E-02 0 0
CUI: C1855514
Disease: Severe failure to thrive
Severe failure to thrive 		14 4 2 8.3E-02 1 0.12
CUI: C1858583
Disease: HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA 		1 0 1 8.3E-02 0 0
CUI: C1859863
Disease: Cerebral cortical neurodegeneration
Cerebral cortical neurodegeneration 		1 0 1 8.3E-02 0 0
CUI: C1876166
Disease: Endemic Tyrolean Infantile Cirrhosis
Endemic Tyrolean Infantile Cirrhosis 		1 0 1 8.3E-02 0 0
CUI: C2675528
Disease: Spastic Paraplegia 42, Autosomal Dominant
Spastic Paraplegia 42, Autosomal Dominant 		1 0 1 8.3E-02 0 0
CUI: C3280965
Disease: CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION
CONGENITAL CATARACTS, HEARING LOSS, AND NEURODEGENERATION 		1 0 1 8.3E-02 0 0
CUI: C3495797
Disease: Peripheral artery stenosis
Peripheral artery stenosis 		1 0 1 8.3E-02 0 0
CUI: C4017428
Disease: CERULOPLASMIN BELFAST PHENOTYPE
CERULOPLASMIN BELFAST PHENOTYPE 		1 0 1 8.3E-02 0 0
CUI: C4022160
Disease: Motheaten muscle fibers
Motheaten muscle fibers 		1 1 1 8.3E-02 1 0.20