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: C0398568
Disease: Blood group deletion syndrome
Blood group deletion syndrome 		7 0 4 0.36 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 2 0.14 0 0
CUI: C0853085
Disease: Decreased LDL cholesterol concentration
Decreased LDL cholesterol concentration 		9 0 2 0.13 0 0
CUI: C0151731
Disease: Hepatic infarction
Hepatic infarction 		1 0 1 0.12 0 0
CUI: C0272405
Disease: Functional asplenia
Functional asplenia 		1 0 1 0.12 0 0
CUI: C0393577
Disease: Pallidal degeneration
Pallidal degeneration 		1 0 1 0.12 0 0
CUI: C0474679
Disease: Serum ceruloplasmin measurement
Serum ceruloplasmin measurement 		1 0 1 0.12 0 0
CUI: C0523509
Disease: Apolipoprotein B Assay
Apolipoprotein B Assay 		1 0 1 0.12 0 0
CUI: C0745868
Disease: lower extremity neuropathy
lower extremity neuropathy 		1 0 1 0.12 0 0
CUI: C0751549
Disease: Neurogenic Thoracic Outlet Syndrome
Neurogenic Thoracic Outlet Syndrome 		1 0 1 0.12 0 0
CUI: C1704299
Disease: Hypobetalipoproteinemia, Familial, Apolipoprotein B
Hypobetalipoproteinemia, Familial, Apolipoprotein B 		1 0 1 0.12 0 0
CUI: C1858583
Disease: HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA 		1 0 1 0.12 0 0
CUI: C1860219
Disease: Self-mutilation of tongue and lips due to involuntary movements
Self-mutilation of tongue and lips due to involuntary movements 		1 0 1 0.12 0 0
CUI: C2751506
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1, ATYPICAL
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1, ATYPICAL 		1 0 1 0.12 0 0
CUI: C3888316
Disease: Hypercholesterolemia, familial, due to ligand-defective apolipoprotein B
Hypercholesterolemia, familial, due to ligand-defective apolipoprotein B 		1 0 1 0.12 0 0
CUI: C4017428
Disease: CERULOPLASMIN BELFAST PHENOTYPE
CERULOPLASMIN BELFAST PHENOTYPE 		1 0 1 0.12 0 0
CUI: C4324627
Disease: Gadolinium deposition disease
Gadolinium deposition disease 		1 0 1 0.12 0 0
CUI: C4510408
Disease: McLeod neuroacanthocytosis syndrome
McLeod neuroacanthocytosis syndrome 		1 0 1 0.12 0 0
CUI: C0002735
Disease: Oppenheim's Disease
Oppenheim's Disease 		2 0 1 0.11 0 0
CUI: C0152457
Disease: Kayser-Fleischer ring
Kayser-Fleischer ring 		2 0 1 0.11 0 0
CUI: C0156847
Disease: Anaemia, postpartum
Anaemia, postpartum 		2 0 1 0.11 0 0
CUI: C0239549
Disease: Fat intolerance
Fat intolerance 		2 0 1 0.11 0 0
CUI: C0268197
Disease: Familial lipoprotein deficiency
Familial lipoprotein deficiency 		2 0 1 0.11 0 0
CUI: C0424323
Disease: Physical aggression
Physical aggression 		2 0 1 0.11 0 0
CUI: C1272174
Disease: Scotopic sensitivity
Scotopic sensitivity 		2 0 1 0.11 0 0