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: C1834582
Disease: MYELOPROLIFERATIVE SYNDROME, TRANSIENT
MYELOPROLIFERATIVE SYNDROME, TRANSIENT 		105 0 52 0.43 0 0
CUI: C0752282
Disease: Congenital Structural Myopathy
Congenital Structural Myopathy 		18 0 14 0.20 0 0
CUI: C3661489
Disease: Autosomal Dominant Myotubular Myopathy
Autosomal Dominant Myotubular Myopathy 		13 0 13 0.19 0 0
CUI: C4551952
Disease: Myopathy, Centronuclear, 1
Myopathy, Centronuclear, 1 		13 0 13 0.19 0 0
CUI: C1834558
Disease: Myopathy, Centronuclear, Autosomal Dominant
Myopathy, Centronuclear, Autosomal Dominant 		16 0 13 0.19 0 0
CUI: C3645536
Disease: Autosomal Recessive Centronuclear Myopathy
Autosomal Recessive Centronuclear Myopathy 		16 0 13 0.19 0 0
CUI: C0410203
Disease: X-linked centronuclear myopathy
X-linked centronuclear myopathy 		29 0 14 0.17 0 0
CUI: C1842170
Disease: Centrally nucleated skeletal muscle fibers
Centrally nucleated skeletal muscle fibers 		25 0 13 0.16 0 0
CUI: C0175709
Disease: Centronuclear myopathy
Centronuclear myopathy 		40 0 14 0.15 0 0
CUI: C0546264
Disease: Congenital Fiber Type Disproportion
Congenital Fiber Type Disproportion 		33 0 13 0.15 0 0
CUI: C3495949
Disease: Locally advanced breast cancer
Locally advanced breast cancer 		71 0 13 0.10 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 10 9.3E-02 0 0
CUI: C0917996
Disease: Cerebral Aneurysm
Cerebral Aneurysm 		65 0 11 9.1E-02 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 6 9.0E-02 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 9 8.8E-02 0 0
CUI: C0333873
Disease: Squamous intraepithelial lesion
Squamous intraepithelial lesion 		73 0 11 8.5E-02 0 0
CUI: C0240805
Disease: Prodrome
Prodrome 		10 0 6 8.5E-02 0 0
CUI: C3808250
Disease: Reduced forced vital capacity
Reduced forced vital capacity 		10 0 6 8.5E-02 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		63 0 10 8.3E-02 0 0
CUI: C0279084
Disease: Kaposi's sarcoma classical type
Kaposi's sarcoma classical type 		26 0 7 8.1E-02 0 0
CUI: C4022583
Disease: Fatiguable weakness of proximal limb muscles
Fatiguable weakness of proximal limb muscles 		14 0 6 8.0E-02 0 0
CUI: C0085923
Disease: soft neurological signs
soft neurological signs 		15 0 6 7.9E-02 0 0
CUI: C3806467
Disease: Respiratory insufficiency due to muscle weakness
Respiratory insufficiency due to muscle weakness 		85 0 11 7.8E-02 0 0
CUI: C1843057
Disease: Calf muscle hypertrophy
Calf muscle hypertrophy 		46 0 8 7.6E-02 0 0
CUI: C0233746
Disease: Perceptual disturbance
Perceptual disturbance 		5 0 5 7.5E-02 0 0