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: C1832525
Disease: Limb-girdle muscular dystrophy type 2F
Limb-girdle muscular dystrophy type 2F 		5 0 3 0.27 0 0
CUI: C2936331
Disease: Sarcoglycanopathies
Sarcoglycanopathies 		20 3 5 0.21 3 5.2E-02
CUI: C1858593
Disease: Limb-girdle muscular dystrophy, type 2E
Limb-girdle muscular dystrophy, type 2E 		5 0 2 0.17 0 0
CUI: C0410173
Disease: Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder)
Severe autosomal recessive muscular dystrophy of childhood - North African type (disorder) 		14 0 3 0.15 0 0
CUI: C1850808
Disease: Miyoshi myopathy
Miyoshi myopathy 		7 0 2 0.14 0 0
CUI: C4551973
Disease: Miyoshi Muscular Dystrophy 1
Miyoshi Muscular Dystrophy 1 		7 0 2 0.14 0 0
CUI: C4554215
Disease: Duchenne or Becker muscular dystrophy
Duchenne or Becker muscular dystrophy 		7 0 2 0.14 0 0
CUI: C0427064
Disease: Pelvic girdle weakness
Pelvic girdle weakness 		16 0 3 0.14 0 0
CUI: C1842552
Disease: Limb-girdle muscle atrophy
Limb-girdle muscle atrophy 		8 0 2 0.13 0 0
CUI: C1839666
Disease: Calf muscle pseudohypertrophy
Calf muscle pseudohypertrophy 		17 0 3 0.13 0 0
CUI: C1869123
Disease: Limb-girdle muscular dystrophy type 2A
Limb-girdle muscular dystrophy type 2A 		18 0 3 0.12 0 0
CUI: C1850889
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B 		19 0 3 0.12 0 0
CUI: C1850794
Disease: Proximal amyotrophy
Proximal amyotrophy 		29 0 4 0.12 0 0
CUI: C0241237
Disease: Difficulty standing
Difficulty standing 		21 0 3 0.11 0 0
CUI: C0454643
Disease: Word finding difficulty (disorder)
Word finding difficulty (disorder) 		1 0 1 0.11 0 0
CUI: C0522055
Disease: Electrocardiogram abnormal
Electrocardiogram abnormal 		11 0 2 0.11 0 0
CUI: C1847532
Disease: MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET
MYOPATHY, DISTAL, WITH ANTERIOR TIBIAL ONSET 		1 0 1 0.11 0 0
CUI: C1858127
Disease: Limb-girdle muscle weakness
Limb-girdle muscle weakness 		41 0 5 0.11 0 0
CUI: C1969029
Disease: Lissencephaly 3
Lissencephaly 3 		1 40 1 0.11 1 1.0E-02
CUI: C2930900
Disease: Beta-sarcoglycanopathy
Beta-sarcoglycanopathy 		1 0 1 0.11 0 0
CUI: C3150413
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 		1 0 1 0.11 0 0
CUI: C4016970
Disease: MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 5
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 5 		1 0 1 0.11 0 0
CUI: C4022625
Disease: Absent muscle fiber calpain-3
Absent muscle fiber calpain-3 		1 0 1 0.11 0 0
CUI: C4022631
Disease: Absent muscle fiber dysferlin
Absent muscle fiber dysferlin 		1 0 1 0.11 0 0
CUI: C4022651
Disease: Reduced muscle fiber merosin
Reduced muscle fiber merosin 		1 0 1 0.11 0 0