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 0.33 0 0
CUI: C0342278
Disease: Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans
Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 		1 0 1 0.33 0 0
CUI: C0343713
Disease: Gonococcal arthritis dermatitis syndrome
Gonococcal arthritis dermatitis syndrome 		1 0 1 0.33 0 0
CUI: C0474679
Disease: Serum ceruloplasmin measurement
Serum ceruloplasmin measurement 		1 0 1 0.33 0 0
CUI: C0744451
Disease: Disseminated infection caused by Neisseria gonorrhoeae
Disseminated infection caused by Neisseria gonorrhoeae 		1 0 1 0.33 0 0
CUI: C1858583
Disease: HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA
HEMOSIDEROSIS, SYSTEMIC, DUE TO ACERULOPLASMINEMIA 		1 0 1 0.33 0 0
CUI: C1864952
Disease: Hyperinsulinemic Hypoglycemia, Familial, 5
Hyperinsulinemic Hypoglycemia, Familial, 5 		1 0 1 0.33 0 0
CUI: C3810402
Disease: ECULIZUMAB, POOR RESPONSE TO
ECULIZUMAB, POOR RESPONSE TO 		1 0 1 0.33 0 0
CUI: C4017428
Disease: CERULOPLASMIN BELFAST PHENOTYPE
CERULOPLASMIN BELFAST PHENOTYPE 		1 0 1 0.33 0 0
CUI: C4024844
Disease: Generalized seborrheic dermatitis
Generalized seborrheic dermatitis 		1 0 1 0.33 0 0
CUI: C0152457
Disease: Kayser-Fleischer ring
Kayser-Fleischer ring 		2 0 1 0.25 0 0
CUI: C0263536
Disease: Hypertrophy of nail
Hypertrophy of nail 		2 0 1 0.25 0 0
CUI: C0271689
Disease: Insulin Receptor, Defect in
Insulin Receptor, Defect in 		2 0 1 0.25 0 0
CUI: C0333244
Disease: Transient edema
Transient edema 		2 0 1 0.25 0 0
CUI: C0342337
Disease: Insulin resistance - type B
Insulin resistance - type B 		2 0 1 0.25 0 0
CUI: C0851883
Disease: Neisseria infection
Neisseria infection 		2 0 1 0.25 0 0
CUI: C1855513
Disease: Prominent nipples
Prominent nipples 		2 0 1 0.25 0 0
CUI: C2931082
Disease: Familial apoceruloplasmin deficiency
Familial apoceruloplasmin deficiency 		2 0 1 0.25 0 0
CUI: C2931429
Disease: Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections
Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal infections 		2 0 1 0.25 0 0
CUI: C0085397
Disease: Pasteurellaceae Infections
Pasteurellaceae Infections 		3 0 1 0.20 0 0
CUI: C0235988
Disease: Serum iron low (finding)
Serum iron low (finding) 		3 0 1 0.20 0 0
CUI: C0342311
Disease: Neuroglycopenia
Neuroglycopenia 		3 0 1 0.20 0 0
CUI: C0854279
Disease: Basal ganglion degeneration
Basal ganglion degeneration 		3 0 1 0.20 0 0
CUI: C0860016
Disease: Fulminant Wilson's disease
Fulminant Wilson's disease 		3 0 1 0.20 0 0
CUI: C1449646
Disease: Primary Peritonitis
Primary Peritonitis 		3 0 1 0.20 0 0