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: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome 		0 3 0 0 1 1.7E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.7E-02
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 1.7E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.6E-02
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.7E-02
CUI: C0342613
Disease: Danish type familial amyloid cardiomyopathy
Danish type familial amyloid cardiomyopathy 		0 2 0 0 1 1.7E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 1.7E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 1.7E-02
CUI: C2750824
Disease: Dystransthyretinemic Euthyroidal Hyperthyroxinemia
Dystransthyretinemic Euthyroidal Hyperthyroxinemia 		0 4 0 0 1 1.6E-02
CUI: C3151471
Disease: AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED
AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED 		0 1 0 0 1 1.7E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.7E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.7E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.7E-02
CUI: C3890602
Disease: Bodily Pain
Bodily Pain 		0 4 0 0 1 1.6E-02
CUI: C4275067
Disease: Transthyretin related familial amyloid cardiomyopathy
Transthyretin related familial amyloid cardiomyopathy 		0 1 0 0 1 1.7E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 1.5E-02
CUI: C4531196
Disease: Transthyretin cardiac amyloidosis
Transthyretin cardiac amyloidosis 		0 2 0 0 1 1.7E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 3.4E-02
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc 		98 0 1 2.0E-03 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 0 1 2.0E-03 0 0
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		82 0 1 2.1E-03 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia 		77 0 1 2.1E-03 0 0
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance 		76 0 1 2.1E-03 0 0
CUI: C4023106
Disease: Obstructive azoospermia
Obstructive azoospermia 		74 0 1 2.1E-03 0 0
CUI: C0034068
Disease: Pulmonary Eosinophilia
Pulmonary Eosinophilia 		70 0 1 2.1E-03 0 0