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: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 0.14 0 0
CUI: C0026244
Disease: Mitochondrial Swelling
Mitochondrial Swelling 		1 0 1 0.14 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 0.14 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 0.14 0 0
CUI: C0345218
Disease: Low anorectal malformation
Low anorectal malformation 		1 0 1 0.14 0 0
CUI: C1836447
Disease: Nemaline myopathy 4
Nemaline myopathy 4 		1 0 1 0.14 0 0
CUI: C1846331
Disease: Juvenile-onset dystonia
Juvenile-onset dystonia 		1 0 1 0.14 0 0
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 11 1 0.14 11 0.73
CUI: C1858042
Disease: Becker Nevus Syndrome
Becker Nevus Syndrome 		1 0 1 0.14 0 0
CUI: C2750413
Disease: Cap Myopathy, Tpm2-Related
Cap Myopathy, Tpm2-Related 		1 0 1 0.14 0 0
CUI: C2936171
Disease: Familial Ebstein's Anomaly
Familial Ebstein's Anomaly 		1 0 1 0.14 0 0
CUI: C3150690
Disease: LEFT VENTRICULAR NONCOMPACTION 5
LEFT VENTRICULAR NONCOMPACTION 5 		1 6 1 0.14 1 5.0E-02
CUI: C3280556
Disease: PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS 		1 0 1 0.14 0 0
CUI: C3807907
Disease: CAP MYOPATHY 2
CAP MYOPATHY 2 		1 0 1 0.14 0 0
CUI: C4016270
Disease: CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC
CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC 		1 0 1 0.14 0 0
CUI: C4023127
Disease: Toe extensor amyotrophy
Toe extensor amyotrophy 		1 0 1 0.14 0 0
CUI: C4023292
Disease: Imperforate tricuspid valve
Imperforate tricuspid valve 		1 0 1 0.14 0 0
CUI: C4275073
Disease: Desmin related myopathy with Mallory body-like inclusions
Desmin related myopathy with Mallory body-like inclusions 		1 0 1 0.14 0 0
CUI: C0011992
Disease: Infantile Diarrhea
Infantile Diarrhea 		2 0 1 0.12 0 0
CUI: C0266833
Disease: Visceral Myopathy, Familial
Visceral Myopathy, Familial 		2 0 1 0.12 0 0
CUI: C0332949
Disease: Overriding structures
Overriding structures 		2 0 1 0.12 0 0
CUI: C1279376
Disease: Inflammatory abdominal aortic aneurysm
Inflammatory abdominal aortic aneurysm 		2 0 1 0.12 0 0
CUI: C1290162
Disease: Disorder of smooth muscle
Disorder of smooth muscle 		2 0 1 0.12 0 0
CUI: C1450052
Disease: Tibial Muscular Dystrophy
Tibial Muscular Dystrophy 		2 0 1 0.12 0 0
CUI: C1527298
Disease: Dysentery, Bacillary
Dysentery, Bacillary 		2 0 1 0.12 0 0