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: C0267494
Disease: Chilaiditi Syndrome
Chilaiditi Syndrome 		1 0 1 1.00 0 0
CUI: C0410165
Disease: X-linked muscular dystrophy with abnormal dystrophin
X-linked muscular dystrophy with abnormal dystrophin 		1 0 1 1.00 0 0
CUI: C0699741
Disease: Benign congenital myopathy
Benign congenital myopathy 		1 0 1 1.00 0 0
CUI: C2875313
Disease: Severe [Duchenne] muscular dystrophy
Severe [Duchenne] muscular dystrophy 		1 0 1 1.00 0 0
CUI: C3844818
Disease: Attention Deficit Hyper Activity
Attention Deficit Hyper Activity 		1 0 1 1.00 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 1.00 0 0
CUI: C4016477
Disease: INTERMEDIATE MUSCULAR DYSTROPHY
INTERMEDIATE MUSCULAR DYSTROPHY 		1 0 1 1.00 0 0
CUI: C0026851
Disease: Muscular Dystrophy, Animal
Muscular Dystrophy, Animal 		2 0 1 0.50 0 0
CUI: C0039223
Disease: Tabes Dorsalis
Tabes Dorsalis 		2 0 1 0.50 0 0
CUI: C0241705
Disease: Difficulty passing urine
Difficulty passing urine 		2 0 1 0.50 0 0
CUI: C0948825
Disease: Systremma
Systremma 		2 0 1 0.50 0 0
CUI: C1540600
Disease: Cerebral seizure
Cerebral seizure 		2 0 1 0.50 0 0
CUI: C0268418
Disease: Deficiency of glycerol kinase
Deficiency of glycerol kinase 		3 0 1 0.33 0 0
CUI: C0456702
Disease: Severe childhood autosomal recessive muscular dystrophy
Severe childhood autosomal recessive muscular dystrophy 		3 0 1 0.33 0 0
CUI: C0587044
Disease: Left ventricular thrombus
Left ventricular thrombus 		3 0 1 0.33 0 0
CUI: C1328551
Disease: Transfusion associated graft versus host disease
Transfusion associated graft versus host disease 		3 0 1 0.33 0 0
CUI: C3668940
Disease: Dmd-Associated Dilated Cardiomyopathy
Dmd-Associated Dilated Cardiomyopathy 		3 0 1 0.33 0 0
CUI: C0410214
Disease: Myopathy with Abnormal Lipid Metabolism
Myopathy with Abnormal Lipid Metabolism 		4 0 1 0.25 0 0
CUI: C1855579
Disease: Exercise-induced muscle stiffness
Exercise-induced muscle stiffness 		4 0 1 0.25 0 0
CUI: C2748527
Disease: KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (disorder)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (disorder) 		4 0 1 0.25 0 0
CUI: C0340434
Disease: Dystrophic cardiomyopathy
Dystrophic cardiomyopathy 		5 0 1 0.20 0 0
CUI: C1858593
Disease: Limb-girdle muscular dystrophy, type 2E
Limb-girdle muscular dystrophy, type 2E 		5 0 1 0.20 0 0
CUI: C1998045
Disease: Subclinical hyperthyroidism
Subclinical hyperthyroidism 		5 0 1 0.20 0 0
CUI: C3203509
Disease: Neuropsychiatric syndrome
Neuropsychiatric syndrome 		6 0 1 0.17 0 0
CUI: C4021526
Disease: Exercise-induced rhabdomyolysis
Exercise-induced rhabdomyolysis 		6 0 1 0.17 0 0