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: C3645536
Disease: Autosomal Recessive Centronuclear Myopathy
Autosomal Recessive Centronuclear Myopathy 		16 0 1 6.2E-02 0 0
CUI: C3805839
Disease: Central hypoventilation
Central hypoventilation 		16 0 1 6.2E-02 0 0
CUI: C4023180
Disease: Type 1 muscle fiber atrophy
Type 1 muscle fiber atrophy 		16 0 1 6.2E-02 0 0
CUI: C0334459
Disease: Infantile fibrosarcoma
Infantile fibrosarcoma 		17 0 1 5.9E-02 0 0
CUI: C1857304
Disease: Flexion contracture of finger
Flexion contracture of finger 		17 0 1 5.9E-02 0 0
CUI: C0752282
Disease: Congenital Structural Myopathy
Congenital Structural Myopathy 		18 0 1 5.6E-02 0 0
CUI: C0334371
Disease: Secretory breast carcinoma
Secretory breast carcinoma 		19 0 1 5.3E-02 0 0
CUI: C4024921
Disease: Lower limb amyotrophy
Lower limb amyotrophy 		19 0 1 5.3E-02 0 0
CUI: C1838114
Disease: Generalized limb muscle atrophy
Generalized limb muscle atrophy 		21 0 1 4.8E-02 0 0
CUI: C1857790
Disease: Thoracic scoliosis
Thoracic scoliosis 		23 0 1 4.3E-02 0 0
CUI: C1332079
Disease: Anaplastic Large Cell Lymphoma, ALK-Positive
Anaplastic Large Cell Lymphoma, ALK-Positive 		25 0 1 4.0E-02 0 0
CUI: C1842170
Disease: Centrally nucleated skeletal muscle fibers
Centrally nucleated skeletal muscle fibers 		25 0 1 4.0E-02 0 0
CUI: C1578482
Disease: Valgus deformities of feet
Valgus deformities of feet 		26 0 1 3.8E-02 0 0
CUI: C0039239
Disease: Sinus Tachycardia
Sinus Tachycardia 		29 0 1 3.4E-02 0 0
CUI: C0410203
Disease: X-linked centronuclear myopathy
X-linked centronuclear myopathy 		29 0 1 3.4E-02 0 0
CUI: C0476408
Disease: Reduced vital capacity
Reduced vital capacity 		29 0 1 3.4E-02 0 0
CUI: C1836451
Disease: Distal lower limb amyotrophy
Distal lower limb amyotrophy 		29 0 1 3.4E-02 0 0
CUI: C0006157
Disease: Breech Presentation
Breech Presentation 		30 0 1 3.3E-02 0 0
CUI: C1850573
Disease: Slender build
Slender build 		31 0 1 3.2E-02 0 0
CUI: C0546264
Disease: Congenital Fiber Type Disproportion
Congenital Fiber Type Disproportion 		33 49 1 3.0E-02 2 4.1E-02
CUI: C1856507
Disease: Bulbar signs
Bulbar signs 		33 0 1 3.0E-02 0 0
CUI: C0019553
Disease: Hip Contracture
Hip Contracture 		34 0 1 2.9E-02 0 0
CUI: C0560346
Disease: Difficulty running
Difficulty running 		38 0 1 2.6E-02 0 0
CUI: C1298820
Disease: Aneurysm of aortic root
Aneurysm of aortic root 		39 0 1 2.6E-02 0 0
CUI: C0175709
Disease: Centronuclear myopathy
Centronuclear myopathy 		40 0 1 2.5E-02 0 0