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: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		0 11 0 0 2 8.9E-03
CUI: C0004277
Disease: Tooth Attrition
Tooth Attrition 		0 5 0 0 1 4.5E-03
CUI: C0004604
Disease: Back Pain
Back Pain 		0 10 0 0 1 4.4E-03
CUI: C0033923
Disease: Psychomotor Performance
Psychomotor Performance 		0 1 0 0 1 4.6E-03
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		0 1 0 0 1 4.6E-03
CUI: C0085293
Disease: Hepatitis E
Hepatitis E 		0 2 0 0 1 4.6E-03
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia 		0 1 0 0 1 4.6E-03
CUI: C0201950
Disease: Cholesterol measurement test
Cholesterol measurement test 		0 3 0 0 1 4.6E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 4.6E-03
CUI: C0340613
Disease: Arterial aneurysm
Arterial aneurysm 		0 2 0 0 1 4.6E-03
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations 		0 3 0 0 1 4.6E-03
CUI: C0730278
Disease: Severe nonproliferative diabetic retinopathy
Severe nonproliferative diabetic retinopathy 		0 3 0 0 1 4.6E-03
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		0 2 0 0 2 9.3E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 4.6E-03
CUI: C1333177
Disease: Lymphoproliferative Disorder of the Skin
Lymphoproliferative Disorder of the Skin 		0 4 0 0 1 4.6E-03
CUI: C2674218
Disease: SPHEROCYTOSIS, TYPE 1 (disorder)
SPHEROCYTOSIS, TYPE 1 (disorder) 		0 16 0 0 1 4.3E-03
CUI: C3665365
Disease: Arteriosclerotic cardiovascular disease, NOS
Arteriosclerotic cardiovascular disease, NOS 		0 5 0 0 1 4.5E-03
CUI: C3890352
Disease: P-Selectin Measurement
P-Selectin Measurement 		0 2 0 0 1 4.6E-03
CUI: C4285890
Disease: Carotid artery calcification
Carotid artery calcification 		0 3 0 0 1 4.6E-03
CUI: C4722224
Disease: Vascular Endothelial Growth Factor Receptor 2 Measurement
Vascular Endothelial Growth Factor Receptor 2 Measurement 		0 2 0 0 1 4.6E-03
CUI: C0006915
Disease: Caplan Syndrome
Caplan Syndrome 		1 0 1 7.2E-03 0 0
CUI: C0014574
Disease: Epiphysitis
Epiphysitis 		1 0 1 7.2E-03 0 0
CUI: C0023869
Disease: Lithiasis
Lithiasis 		1 0 1 7.2E-03 0 0
CUI: C0024588
Disease: Malignant essential hypertension
Malignant essential hypertension 		1 0 1 7.2E-03 0 0
CUI: C0030625
Disease: Passive Cutaneous Anaphylaxis
Passive Cutaneous Anaphylaxis 		1 0 1 7.2E-03 0 0