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: C1848456
Disease: Atypical or prolonged hepatitis
Atypical or prolonged hepatitis 		1 0 1 1.00 0 0
CUI: C3495797
Disease: Peripheral artery stenosis
Peripheral artery stenosis 		1 0 1 1.00 0 0
CUI: C4024907
Disease: Mixed demyelinating and axonal polyneuropathy
Mixed demyelinating and axonal polyneuropathy 		1 0 1 1.00 0 0
CUI: C0152457
Disease: Kayser-Fleischer ring
Kayser-Fleischer ring 		2 0 1 0.50 0 0
CUI: C1848459
Disease: High nonceruloplasmin-bound serum copper
High nonceruloplasmin-bound serum copper 		3 0 1 0.33 0 0
CUI: C3151080
Disease: COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II
COMPLEMENT COMPONENT 8 DEFICIENCY, TYPE II 		3 0 1 0.33 0 0
CUI: C0012714
Disease: Disorder of copper metabolism
Disorder of copper metabolism 		5 0 1 0.20 0 0
CUI: C1848453
Disease: Poor motor coordination
Poor motor coordination 		6 0 1 0.17 0 0
CUI: C0312420
Disease: Hypersexuality state
Hypersexuality state 		8 0 1 0.12 0 0
CUI: C0878682
Disease: Ceruloplasmin deficiency
Ceruloplasmin deficiency 		8 0 1 0.12 0 0
CUI: C0015503
Disease: Factor VII Deficiency
Factor VII Deficiency 		10 0 1 1.0E-01 0 0
CUI: C1282975
Disease: von Willebrand Disease, Type 2N
von Willebrand Disease, Type 2N 		10 0 1 1.0E-01 0 0
CUI: C4025888
Disease: Abnormality of the menstrual cycle
Abnormality of the menstrual cycle 		11 0 1 9.1E-02 0 0
CUI: C0240997
Disease: Decreased serum ceruloplasmin
Decreased serum ceruloplasmin 		12 0 1 8.3E-02 0 0
CUI: C0302332
Disease: Poisoning syndrome
Poisoning syndrome 		14 0 1 7.1E-02 0 0
CUI: C0302280
Disease: Adrenogenital Syndrome
Adrenogenital Syndrome 		16 0 1 6.2E-02 0 0
CUI: C0018809
Disease: Heart Neoplasm
Heart Neoplasm 		17 0 1 5.9E-02 0 0
CUI: C0022716
Disease: Menkes Kinky Hair Syndrome
Menkes Kinky Hair Syndrome 		20 0 1 5.0E-02 0 0
CUI: C0268070
Disease: Hypocupremia
Hypocupremia 		23 0 1 4.3E-02 0 0
CUI: C0598784
Disease: Dyslipoproteinemias
Dyslipoproteinemias 		24 0 1 4.2E-02 0 0
CUI: C1527352
Disease: Hepatic Form of Wilson Disease
Hepatic Form of Wilson Disease 		24 0 1 4.2E-02 0 0
CUI: C2169806
Disease: recurrent muscle twitches (symptom)
recurrent muscle twitches (symptom) 		26 0 1 3.8E-02 0 0
CUI: C1866010
Disease: Proximal muscle weakness in lower limbs
Proximal muscle weakness in lower limbs 		30 0 1 3.3E-02 0 0
CUI: C0239842
Disease: Tremor of hands
Tremor of hands 		31 0 1 3.2E-02 0 0
CUI: C0278076
Disease: Behavioral tic
Behavioral tic 		31 0 1 3.2E-02 0 0