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: C0423772
Disease: Cutaneous Fistula
Cutaneous Fistula 		1 0 1 9.1E-02 0 0
CUI: C1719796
Disease: With-the-rule astigmatism
With-the-rule astigmatism 		1 0 1 9.1E-02 0 0
CUI: C4014584
Disease: BLEEDING DISORDER, PLATELET-TYPE, 18
BLEEDING DISORDER, PLATELET-TYPE, 18 		1 0 1 9.1E-02 0 0
CUI: C4025198
Disease: Recurrent gram-negative bacterial infections
Recurrent gram-negative bacterial infections 		1 0 1 9.1E-02 0 0
CUI: C0023510
Disease: Leukocyte Disorders
Leukocyte Disorders 		2 0 1 8.3E-02 0 0
CUI: C0424492
Disease: Coarse features
Coarse features 		2 0 1 8.3E-02 0 0
CUI: C1853120
Disease: Noonan Syndrome 4
Noonan Syndrome 4 		2 0 1 8.3E-02 0 0
CUI: C4024862
Disease: Recurrent staphylococcal infections
Recurrent staphylococcal infections 		2 0 1 8.3E-02 0 0
CUI: C4551558
Disease: Fibromatosis, Gingival, Type 1
Fibromatosis, Gingival, Type 1 		2 0 1 8.3E-02 0 0
CUI: C0149727
Disease: Abnormality of the lymph nodes
Abnormality of the lymph nodes 		3 0 1 7.7E-02 0 0
CUI: C0178829
Disease: reproductive system disorder
reproductive system disorder 		3 0 1 7.7E-02 0 0
CUI: C0340319
Disease: Posterior myocardial infarction
Posterior myocardial infarction 		3 0 1 7.7E-02 0 0
CUI: C0729842
Disease: Serpiginous choroiditis
Serpiginous choroiditis 		3 0 1 7.7E-02 0 0
CUI: C0741183
Disease: aortic stenosis symptomatic
aortic stenosis symptomatic 		3 0 1 7.7E-02 0 0
CUI: C4087338
Disease: Mite allergy
Mite allergy 		3 0 1 7.7E-02 0 0
CUI: C0264695
Disease: Subendocardial ischemia
Subendocardial ischemia 		4 0 1 7.1E-02 0 0
CUI: C1306878
Disease: Climacteric discomfort
Climacteric discomfort 		4 0 1 7.1E-02 0 0
CUI: C1845609
Disease: Lymphoid depletion
Lymphoid depletion 		4 0 1 7.1E-02 0 0
CUI: C3179239
Disease: Osteopetrosis Autosomal Dominant Type 2
Osteopetrosis Autosomal Dominant Type 2 		4 0 1 7.1E-02 0 0
CUI: C3645711
Disease: Congenital Osteopetrosis
Congenital Osteopetrosis 		4 0 1 7.1E-02 0 0
CUI: C4022662
Disease: Abnormality of lateral ventricle
Abnormality of lateral ventricle 		4 0 1 7.1E-02 0 0
CUI: C4024165
Disease: Prominent ear helix
Prominent ear helix 		4 0 1 7.1E-02 0 0
CUI: C0263428
Disease: Burnett Schwartz Berberian syndrome
Burnett Schwartz Berberian syndrome 		5 0 1 6.7E-02 0 0
CUI: C0497299
Disease: meningitis/encephalitis
meningitis/encephalitis 		5 0 1 6.7E-02 0 0
CUI: C1333125
Disease: combined type small cell lung cancer
combined type small cell lung cancer 		5 0 1 6.7E-02 0 0