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: C0151731
Disease: Hepatic infarction
Hepatic infarction 		1 0 1 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: 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
CUI: C4022944
Disease: Abnormal protein N-linked glycosylation
Abnormal protein N-linked glycosylation 		1 0 1 8.3E-02 0 0
CUI: C4023055
Disease: Abnormality of central motor conduction
Abnormality of central motor conduction 		1 0 1 8.3E-02 0 0
CUI: C4024907
Disease: Mixed demyelinating and axonal polyneuropathy
Mixed demyelinating and axonal polyneuropathy 		1 0 1 8.3E-02 0 0
CUI: C4073164
Disease: Decreased urinary copper concentration
Decreased urinary copper concentration 		1 1 1 8.3E-02 1 0.20
CUI: C4225153
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1 		1 0 1 8.3E-02 0 0
CUI: C4225190
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIp
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIp 		1 0 1 8.3E-02 0 0
CUI: C4225191
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIo
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIo 		1 0 1 8.3E-02 0 0
CUI: C4310819
Disease: IMMUNODEFICIENCY 47
IMMUNODEFICIENCY 47 		1 5 1 8.3E-02 1 0.11
CUI: C4479353
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIq 		1 0 1 8.3E-02 0 0
CUI: C4732750
Disease: Decreased hemoglobin concentration
Decreased hemoglobin concentration 		1 0 1 8.3E-02 0 0