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: C0751268
Disease: Encephalopathy, Subacute Necrotizing, Juvenile
Encephalopathy, Subacute Necrotizing, Juvenile 		9 0 3 7.9E-02 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 14 7.5E-02 0 0
CUI: C1404837
Disease: Drug-induced Nephropathy
Drug-induced Nephropathy 		12 0 3 7.3E-02 0 0
CUI: C0086648
Disease: MPS III B
MPS III B 		13 0 3 7.1E-02 0 0
CUI: C0522051
Disease: Acute chest pain
Acute chest pain 		13 0 3 7.1E-02 0 0
CUI: C1704375
Disease: Hypophosphatemic Rickets
Hypophosphatemic Rickets 		29 0 4 7.0E-02 0 0
CUI: C0020599
Disease: Hypocalciuria
Hypocalciuria 		16 0 3 6.7E-02 0 0
CUI: C1850597
Disease: Leigh Syndrome Due To Mitochondrial Complex II Deficiency
Leigh Syndrome Due To Mitochondrial Complex II Deficiency 		36 0 4 6.2E-02 0 0
CUI: C1850598
Disease: Leigh Syndrome due to Mitochondrial Complex III Deficiency
Leigh Syndrome due to Mitochondrial Complex III Deficiency 		36 0 4 6.2E-02 0 0
CUI: C1850600
Disease: Leigh Syndrome due to Mitochondrial Complex V Deficiency
Leigh Syndrome due to Mitochondrial Complex V Deficiency 		36 0 4 6.2E-02 0 0
CUI: C2931891
Disease: Necrotizing encephalopathy, infantile subacute, of Leigh
Necrotizing encephalopathy, infantile subacute, of Leigh 		36 0 4 6.2E-02 0 0
CUI: C4551503
Disease: FANCONI RENOTUBULAR SYNDROME 1
FANCONI RENOTUBULAR SYNDROME 1 		2 0 2 6.2E-02 0 0
CUI: C0028860
Disease: Oculocerebrorenal Syndrome
Oculocerebrorenal Syndrome 		54 0 5 6.2E-02 0 0
CUI: C1850599
Disease: Leigh Syndrome due to Mitochondrial Complex IV Deficiency
Leigh Syndrome due to Mitochondrial Complex IV Deficiency 		37 0 4 6.2E-02 0 0
CUI: C0035579
Disease: Rickets
Rickets 		72 0 6 6.1E-02 0 0
CUI: C1833104
Disease: DIABETES MELLITUS, PERMANENT NEONATAL
DIABETES MELLITUS, PERMANENT NEONATAL 		20 0 3 6.1E-02 0 0
CUI: C0032617
Disease: Polyuria
Polyuria 		73 0 6 6.1E-02 0 0
CUI: C0240928
Disease: Salt craving
Salt craving 		3 0 2 6.1E-02 0 0
CUI: C0520887
Disease: ST segment depression (finding)
ST segment depression (finding) 		3 0 2 6.1E-02 0 0
CUI: C1969408
Disease: Prominent U wave
Prominent U wave 		3 0 2 6.1E-02 0 0
CUI: C4021103
Disease: Abnormality of exocrine pancreas physiology
Abnormality of exocrine pancreas physiology 		3 0 2 6.1E-02 0 0
CUI: C4551898
Disease: Cholestasis, progressive familial intrahepatic 1
Cholestasis, progressive familial intrahepatic 1 		38 0 4 6.1E-02 0 0
CUI: C4551504
Disease: Oculocutaneous albinism type 1A
Oculocutaneous albinism type 1A 		21 0 3 6.0E-02 0 0
CUI: C0271728
Disease: Secondary hyperaldosteronism
Secondary hyperaldosteronism 		4 0 2 5.9E-02 0 0
CUI: C1838951
Disease: LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY 		40 0 4 5.9E-02 0 0