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: C0240997
Disease: Decreased serum ceruloplasmin
Decreased serum ceruloplasmin 		12 5 6 0.21 2 0.40
CUI: C0012714
Disease: Disorder of copper metabolism
Disorder of copper metabolism 		5 0 4 0.17 0 0
CUI: C0022716
Disease: Menkes Kinky Hair Syndrome
Menkes Kinky Hair Syndrome 		20 0 5 0.13 0 0
CUI: C1836330
Disease: ERYTHROKERATODERMIA VARIABILIS 3 (disorder)
ERYTHROKERATODERMIA VARIABILIS 3 (disorder) 		3 0 3 0.13 0 0
CUI: C1527352
Disease: Hepatic Form of Wilson Disease
Hepatic Form of Wilson Disease 		24 0 5 0.12 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 3 0.11 0 0
CUI: C0149519
Disease: Chronic Persistent Hepatitis
Chronic Persistent Hepatitis 		33 0 5 9.8E-02 0 0
CUI: C0524611
Disease: Cryptogenic Chronic Hepatitis
Cryptogenic Chronic Hepatitis 		22 0 4 9.8E-02 0 0
CUI: C0029810
Disease: Other specified iron deficiency anemias
Other specified iron deficiency anemias 		13 0 3 9.1E-02 0 0
CUI: C0302332
Disease: Poisoning syndrome
Poisoning syndrome 		14 0 3 8.8E-02 0 0
CUI: C0152457
Disease: Kayser-Fleischer ring
Kayser-Fleischer ring 		2 0 2 8.7E-02 0 0
CUI: C4524077
Disease: Hypertrophic olivary degeneration
Hypertrophic olivary degeneration 		2 0 2 8.7E-02 0 0
CUI: C0012715
Disease: Iron Metabolism Disorders
Iron Metabolism Disorders 		15 0 3 8.6E-02 0 0
CUI: C0872218
Disease: MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME
MITOCHONDRIAL NEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME 		4 0 2 8.0E-02 0 0
CUI: C2931928
Disease: Mitochondrial cytopathy
Mitochondrial cytopathy 		4 0 2 8.0E-02 0 0
CUI: C4551995
Disease: Mitochondrial DNA Depletion Syndrome 1
Mitochondrial DNA Depletion Syndrome 1 		4 0 2 8.0E-02 0 0
CUI: C0750940
Disease: Tremor, Rubral
Tremor, Rubral 		18 0 3 7.9E-02 0 0
CUI: C1735608
Disease: SLE flare
SLE flare 		5 0 2 7.7E-02 0 0
CUI: C0019054
Disease: Hemolysis (disorder)
Hemolysis (disorder) 		6 0 2 7.4E-02 0 0
CUI: C0312854
Disease: Extravascular Hemolysis
Extravascular Hemolysis 		6 0 2 7.4E-02 0 0
CUI: C0549357
Disease: Abdominal adhesions
Abdominal adhesions 		6 0 2 7.4E-02 0 0
CUI: C1858424
Disease: Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency
Cardioencephalomyopathy, Fatal Infantile, due to Cytochrome C Oxidase Deficiency 		6 0 2 7.4E-02 0 0
CUI: C4022762
Disease: Elevated brain lactate level by MRS
Elevated brain lactate level by MRS 		7 0 2 7.1E-02 0 0
CUI: C3469186
Disease: HEMOCHROMATOSIS, TYPE 1
HEMOCHROMATOSIS, TYPE 1 		83 0 7 7.1E-02 0 0
CUI: C0019114
Disease: Hemosiderosis
Hemosiderosis 		8 0 2 6.9E-02 0 0