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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 1.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.1E-02
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 1.1E-02
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.1E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 1.1E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 1.1E-02
CUI: C0494491
Disease: Mononeuropathies
Mononeuropathies 		0 2 0 0 1 1.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.1E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.0E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.1E-02
CUI: C3501843
Disease: Nonmedullary Thyroid Carcinoma
Nonmedullary Thyroid Carcinoma 		89 0 1 1.1E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.1E-03 0 0
CUI: C1527366
Disease: Salaam Seizures
Salaam Seizures 		75 0 1 1.1E-03 0 0
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
Familial Nonmedullary Thyroid Cancer 		66 0 1 1.1E-03 0 0
CUI: C1836150
Disease: Gait imbalance
Gait imbalance 		57 0 1 1.1E-03 0 0
CUI: C1858036
Disease: Periorbital fullness
Periorbital fullness 		57 0 1 1.1E-03 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		50 0 1 1.1E-03 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 1 1.1E-03 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 1.1E-03 0 0
CUI: C4551564
Disease: Narrow nasal bridge
Narrow nasal bridge 		47 0 1 1.1E-03 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 1 1.1E-03 0 0
CUI: C1868720
Disease: Periventricular Nodular Heterotopia
Periventricular Nodular Heterotopia 		45 0 1 1.1E-03 0 0
CUI: C0332615
Disease: Myopathic facies
Myopathic facies 		44 0 1 1.1E-03 0 0
CUI: C1836308
Disease: Generalized joint laxity
Generalized joint laxity 		44 0 1 1.1E-03 0 0
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		42 0 1 1.1E-03 0 0