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: C0020538
Disease: Hypertensive disease
Hypertensive disease 		2322 1085 111 4.5E-02 1 8.7E-04
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		2803 824 123 4.2E-02 1 1.1E-03
CUI: C0010674
Disease: Cystic Fibrosis
Cystic Fibrosis 		852 704 49 4.5E-02 1 1.3E-03
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		685 663 39 4.2E-02 1 1.4E-03
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		560 635 48 6.1E-02 1 1.4E-03
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		939 584 58 5.0E-02 1 1.5E-03
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 579 61 5.1E-02 1 1.6E-03
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		512 509 61 8.3E-02 2 3.5E-03
CUI: C1855465
Disease: STARGARDT DISEASE 1 (disorder)
STARGARDT DISEASE 1 (disorder) 		23 317 2 6.6E-03 1 2.6E-03
CUI: C1858763
Disease: Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1g 		2 308 2 7.1E-03 1 2.7E-03
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		925 294 109 9.9E-02 1 2.8E-03
CUI: C1850569
Disease: Nemaline Myopathy 2
Nemaline Myopathy 2 		2 265 2 7.1E-03 1 3.0E-03
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		362 247 20 3.2E-02 1 3.2E-03
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 246 3 6.9E-03 1 3.2E-03
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic 		773 243 63 6.4E-02 4 1.3E-02
CUI: C1837342
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2J 		2 230 2 7.1E-03 1 3.4E-03
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 227 18 3.7E-02 1 3.4E-03
CUI: C0030193
Disease: Pain
Pain 		1554 196 80 4.6E-02 1 3.8E-03
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		375 170 101 0.18 3 1.3E-02
CUI: C0026848
Disease: Myopathy
Myopathy 		634 166 122 0.15 5 2.2E-02
CUI: C1850889
Disease: MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B 		19 150 10 3.5E-02 4 1.9E-02
CUI: C1869123
Disease: Limb-girdle muscular dystrophy type 2A
Limb-girdle muscular dystrophy type 2A 		18 146 13 4.6E-02 4 1.9E-02
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
Hereditary Motor and Sensory-Neuropathy Type II 		48 144 4 1.2E-02 4 1.9E-02
CUI: C2315100
Disease: Pediatric failure to thrive
Pediatric failure to thrive 		166 122 9 2.1E-02 1 5.3E-03
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 120 30 4.3E-02 1 5.4E-03