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: C1850674
Disease: MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (disorder)
MINICORE MYOPATHY WITH EXTERNAL OPHTHALMOPLEGIA (disorder) 		11 0 4 0.17 0 0
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		46 0 9 0.17 0 0
CUI: C1836599
Disease: Macrocephaly at birth
Macrocephaly at birth 		12 0 4 0.17 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 11 0.16 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 9 0.16 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity 		29 0 6 0.15 0 0
CUI: C4022591
Disease: Fatigable weakness of bulbar muscles
Fatigable weakness of bulbar muscles 		14 0 4 0.15 0 0
CUI: C0546125
Disease: Nemaline Myopathy, Childhood Onset
Nemaline Myopathy, Childhood Onset 		7 0 3 0.15 0 0
CUI: C0751657
Disease: Nemaline Myopathy, Autosomal Recessive
Nemaline Myopathy, Autosomal Recessive 		7 0 3 0.15 0 0
CUI: C1842160
Disease: MYOPATHY, MYOSIN STORAGE (disorder)
MYOPATHY, MYOSIN STORAGE (disorder) 		7 0 3 0.15 0 0
CUI: C0560346
Disease: Difficulty running
Difficulty running 		38 0 7 0.15 0 0
CUI: C3808039
Disease: Nemaline bodies
Nemaline bodies 		15 0 4 0.15 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 9 0.15 0 0
CUI: C0270962
Disease: Multi-core congenital myopathy
Multi-core congenital myopathy 		16 0 4 0.14 0 0
CUI: C1857304
Disease: Flexion contracture of finger
Flexion contracture of finger 		17 0 4 0.14 0 0
CUI: C1836003
Disease: Facial diplegia
Facial diplegia 		42 0 7 0.14 0 0
CUI: C1389113
Disease: Generalized amyotrophy
Generalized amyotrophy 		56 0 8 0.12 0 0
CUI: C1446787
Disease: Cramping sensation quality
Cramping sensation quality 		2 0 2 0.12 0 0
CUI: C1450052
Disease: Tibial Muscular Dystrophy
Tibial Muscular Dystrophy 		2 0 2 0.12 0 0
CUI: C4025568
Disease: Type 1 and type 2 muscle fiber minicore regions
Type 1 and type 2 muscle fiber minicore regions 		2 0 2 0.12 0 0
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 11 0.12 0 0
CUI: C1866010
Disease: Proximal muscle weakness in lower limbs
Proximal muscle weakness in lower limbs 		30 0 5 0.12 0 0
CUI: C1838114
Disease: Generalized limb muscle atrophy
Generalized limb muscle atrophy 		21 0 4 0.12 0 0
CUI: C0240479
Disease: Neck muscle weakness
Neck muscle weakness 		49 0 7 0.12 0 0
CUI: C4025729
Disease: Neuromuscular dysphagia
Neuromuscular dysphagia 		12 0 3 0.12 0 0