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: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 5.0E-02
CUI: C1511306
Disease: Breast Diffuse Large B-Cell Lymphoma
Breast Diffuse Large B-Cell Lymphoma 		0 1 0 0 1 5.0E-02
CUI: C4749271
Disease: Aleukemic mast cell leukemia
Aleukemic mast cell leukemia 		0 2 0 0 2 1.0E-01
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		264 0 1 1.7E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 1.8E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 1.9E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 2.0E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 2.0E-03 0 0
CUI: C3468561
Disease: familial atrial fibrillation
familial atrial fibrillation 		157 0 1 2.0E-03 0 0
CUI: C2585653
Disease: Persistent atrial fibrillation
Persistent atrial fibrillation 		156 0 1 2.0E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 2.1E-03 0 0
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death 		133 0 1 2.1E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 2.2E-03 0 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		126 0 1 2.2E-03 0 0
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		124 0 1 2.2E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 2.2E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 2.2E-03 0 0
CUI: C4552811
Disease: Generalized Muscle Weakness, CTCAE
Generalized Muscle Weakness, CTCAE 		117 0 1 2.2E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		113 0 1 2.2E-03 0 0
CUI: C0231712
Disease: Waddling gait
Waddling gait 		113 0 1 2.2E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 0 1 2.2E-03 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures 		105 0 1 2.3E-03 0 0
CUI: C0598589
Disease: Inherited neuropathies
Inherited neuropathies 		104 0 1 2.3E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc 		98 0 1 2.3E-03 0 0
CUI: C0013132
Disease: Drooling
Drooling 		95 0 1 2.3E-03 0 0