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: C1842161
Disease: Scapuloperoneal weakness
Scapuloperoneal weakness 		3 0 2 0.50 0 0
CUI: C0333062
Disease: Hernia sac
Hernia sac 		1 0 1 0.33 0 0
CUI: C1846010
Disease: URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME 		1 0 1 0.33 0 0
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 0 1 0.33 0 0
CUI: C2678015
Disease: Myopathy, Reducing Body, X-Linked, Childhood-Onset
Myopathy, Reducing Body, X-Linked, Childhood-Onset 		1 0 1 0.33 0 0
CUI: C2678027
Disease: Myopathy, Reducing Body, X-Linked, Early-Onset, Severe
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe 		1 0 1 0.33 0 0
CUI: C2678055
Disease: MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder)
MYOPATHY, X-LINKED, WITH POSTURAL MUSCLE ATROPHY (disorder) 		1 0 1 0.33 0 0
CUI: C2749106
Disease: Emery-Dreifuss Muscular Dystrophy 6, X-Linked
Emery-Dreifuss Muscular Dystrophy 6, X-Linked 		1 0 1 0.33 0 0
CUI: C2750536
Disease: Nemaline Myopathy 3, With Intranuclear Rods
Nemaline Myopathy 3, With Intranuclear Rods 		1 0 1 0.33 0 0
CUI: C2750537
Disease: Myopathy, Actin, Congenital, With Cores
Myopathy, Actin, Congenital, With Cores 		1 0 1 0.33 0 0
CUI: C2936171
Disease: Familial Ebstein's Anomaly
Familial Ebstein's Anomaly 		1 0 1 0.33 0 0
CUI: C3150690
Disease: LEFT VENTRICULAR NONCOMPACTION 5
LEFT VENTRICULAR NONCOMPACTION 5 		1 0 1 0.33 0 0
CUI: C4016270
Disease: CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC
CARDIOMYOPATHY, HYPERTROPHIC, MIDVENTRICULAR, DIGENIC 		1 0 1 0.33 0 0
CUI: C4023127
Disease: Toe extensor amyotrophy
Toe extensor amyotrophy 		1 0 1 0.33 0 0
CUI: C4023292
Disease: Imperforate tricuspid valve
Imperforate tricuspid valve 		1 0 1 0.33 0 0
CUI: C4225159
Disease: REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET
REDUCING BODY MYOPATHY, X-LINKED 1B, WITH LATE CHILDHOOD OR ADULT ONSET 		1 0 1 0.33 0 0
CUI: C4225181
Disease: MYOPATHY, SCAPULOHUMEROPERONEAL
MYOPATHY, SCAPULOHUMEROPERONEAL 		1 0 1 0.33 0 0
CUI: C4225423
Disease: REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET
REDUCING BODY MYOPATHY, X-LINKED 1A, SEVERE, WITH INFANTILE OR EARLY CHILDHOOD ONSET 		1 0 1 0.33 0 0
CUI: C4025571
Disease: Type 1 fibers relatively smaller than type 2 fibers
Type 1 fibers relatively smaller than type 2 fibers 		6 0 2 0.29 0 0
CUI: C0231666
Disease: Wrist-Drop
Wrist-Drop 		2 0 1 0.25 0 0
CUI: C1450052
Disease: Tibial Muscular Dystrophy
Tibial Muscular Dystrophy 		2 0 1 0.25 0 0
CUI: C1839030
Disease: Weakness of orbicularis oculi muscle
Weakness of orbicularis oculi muscle 		2 0 1 0.25 0 0
CUI: C1846011
Disease: Pugilistic facies
Pugilistic facies 		2 0 1 0.25 0 0
CUI: C3711377
Disease: Intranuclear Rod Myopathy
Intranuclear Rod Myopathy 		2 0 1 0.25 0 0
CUI: C3711389
Disease: Actin-Accumulation Myopathy
Actin-Accumulation Myopathy 		2 0 1 0.25 0 0