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: C0948825
Disease: Systremma
Systremma 		2 0 2 0.67 0 0
CUI: C0587044
Disease: Left ventricular thrombus
Left ventricular thrombus 		3 0 2 0.50 0 0
CUI: C1328551
Disease: Transfusion associated graft versus host disease
Transfusion associated graft versus host disease 		3 0 2 0.50 0 0
CUI: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 0.33 0 0
CUI: C0271149
Disease: Secondary angle-closure glaucoma
Secondary angle-closure glaucoma 		1 0 1 0.33 0 0
CUI: C0271152
Disease: Malignant glaucoma
Malignant glaucoma 		1 0 1 0.33 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 0.33 0 0
CUI: C0677500
Disease: Stinging Sensation
Stinging Sensation 		1 0 1 0.33 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 0.33 0 0
CUI: C1720732
Disease: Subretinal fluid (finding)
Subretinal fluid (finding) 		1 0 1 0.33 0 0
CUI: C1998045
Disease: Subclinical hyperthyroidism
Subclinical hyperthyroidism 		5 0 2 0.33 0 0
CUI: C2678493
Disease: BESTROPHINOPATHY
BESTROPHINOPATHY 		1 0 1 0.33 0 0
CUI: C2750789
Disease: RETINITIS PIGMENTOSA, CONCENTRIC (disorder)
RETINITIS PIGMENTOSA, CONCENTRIC (disorder) 		1 0 1 0.33 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 0.33 0 0
CUI: C3844818
Disease: Attention Deficit Hyper Activity
Attention Deficit Hyper Activity 		1 0 1 0.33 0 0
CUI: C4016476
Disease: DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE
DUCHENNE MUSCULAR DYSTROPHY, MENTAL RETARDATION, AND ABSENCE OF ERG B-WAVE 		1 0 1 0.33 0 0
CUI: C4016477
Disease: INTERMEDIATE MUSCULAR DYSTROPHY
INTERMEDIATE MUSCULAR DYSTROPHY 		1 0 1 0.33 0 0
CUI: C4022648
Disease: Abnormal muscle fiber dystrophin expression
Abnormal muscle fiber dystrophin expression 		1 0 1 0.33 0 0
CUI: C4024761
Disease: Retinal arteriolar occlusion
Retinal arteriolar occlusion 		1 0 1 0.33 0 0
CUI: C4024819
Disease: Abnormality of chorioretinal pigmentation
Abnormality of chorioretinal pigmentation 		1 0 1 0.33 0 0
CUI: C0026851
Disease: Muscular Dystrophy, Animal
Muscular Dystrophy, Animal 		2 0 1 0.25 0 0
CUI: C0039223
Disease: Tabes Dorsalis
Tabes Dorsalis 		2 0 1 0.25 0 0
CUI: C0241705
Disease: Difficulty passing urine
Difficulty passing urine 		2 0 1 0.25 0 0
CUI: C0271004
Disease: Absent anterior chamber of eye
Absent anterior chamber of eye 		2 0 1 0.25 0 0
CUI: C1540600
Disease: Cerebral seizure
Cerebral seizure 		2 0 1 0.25 0 0