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: C3711377
Disease: Intranuclear Rod Myopathy
Intranuclear Rod Myopathy 		2 0 2 1.00 0 0
CUI: C0270992
Disease: Secondary myopathy
Secondary myopathy 		3 0 2 0.67 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 0.50 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 0.50 0 0
CUI: C0270969
Disease: Zebra body myopathy
Zebra body myopathy 		4 0 2 0.50 0 0
CUI: C0751656
Disease: Nemaline Myopathy, Autosomal Dominant
Nemaline Myopathy, Autosomal Dominant 		4 0 2 0.50 0 0
CUI: C1846331
Disease: Juvenile-onset dystonia
Juvenile-onset dystonia 		1 0 1 0.50 0 0
CUI: C1858042
Disease: Becker Nevus Syndrome
Becker Nevus Syndrome 		1 0 1 0.50 0 0
CUI: C2750536
Disease: Nemaline Myopathy 3, With Intranuclear Rods
Nemaline Myopathy 3, With Intranuclear Rods 		1 0 1 0.50 0 0
CUI: C2750537
Disease: Myopathy, Actin, Congenital, With Cores
Myopathy, Actin, Congenital, With Cores 		1 2 1 0.50 2 4.2E-02
CUI: C4225181
Disease: MYOPATHY, SCAPULOHUMEROPERONEAL
MYOPATHY, SCAPULOHUMEROPERONEAL 		1 2 1 0.50 1 2.0E-02
CUI: C0011992
Disease: Infantile Diarrhea
Infantile Diarrhea 		2 0 1 0.33 0 0
CUI: C0231666
Disease: Wrist-Drop
Wrist-Drop 		2 0 1 0.33 0 0
CUI: C0266833
Disease: Visceral Myopathy, Familial
Visceral Myopathy, Familial 		2 0 1 0.33 0 0
CUI: C1290162
Disease: Disorder of smooth muscle
Disorder of smooth muscle 		2 0 1 0.33 0 0
CUI: C1527298
Disease: Dysentery, Bacillary
Dysentery, Bacillary 		2 0 1 0.33 0 0
CUI: C1837819
Disease: Cerebrofrontofacial Syndrome
Cerebrofrontofacial Syndrome 		2 0 1 0.33 0 0
CUI: C1844696
Disease: OTOPALATODIGITAL SYNDROME, TYPE II
OTOPALATODIGITAL SYNDROME, TYPE II 		2 0 1 0.33 0 0
CUI: C1846339
Disease: Externally rotated hips
Externally rotated hips 		2 0 1 0.33 0 0
CUI: C3839205
Disease: Signet-ring stromal tumor
Signet-ring stromal tumor 		2 0 1 0.33 0 0
CUI: C4477072
Disease: Iris flocculi
Iris flocculi 		2 0 1 0.33 0 0
CUI: C0751657
Disease: Nemaline Myopathy, Autosomal Recessive
Nemaline Myopathy, Autosomal Recessive 		7 0 2 0.29 0 0
CUI: C0014040
Disease: Encephalitis Lethargica
Encephalitis Lethargica 		3 0 1 0.25 0 0
CUI: C1834339
Disease: Myopathy, Actin, Congenital, with Excess of Thin Myofilaments
Myopathy, Actin, Congenital, with Excess of Thin Myofilaments 		3 1 1 0.25 1 2.1E-02
CUI: C1853623
Disease: Fryns-Aftimos Syndrome
Fryns-Aftimos Syndrome 		3 0 1 0.25 0 0