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: C3250443
Disease: MYOTONIC DYSTROPHY 1
MYOTONIC DYSTROPHY 1 		179 14 53 0.19 1 5.9E-02
CUI: C3811918
Disease: GRN-related frontotemporal dementia
GRN-related frontotemporal dementia 		112 0 20 8.1E-02 0 0
CUI: C0236642
Disease: Pick Disease of the Brain
Pick Disease of the Brain 		213 0 27 7.9E-02 0 0
CUI: C0917713
Disease: Becker Muscular Dystrophy
Becker Muscular Dystrophy 		86 0 17 7.6E-02 0 0
CUI: C3887938
Disease: Deuteranomaly
Deuteranomaly 		92 0 17 7.4E-02 0 0
CUI: C0282513
Disease: Primary Progressive Aphasia (disorder)
Primary Progressive Aphasia (disorder) 		51 0 14 7.3E-02 0 0
CUI: C2931689
Disease: Dystrophia myotonica 2
Dystrophia myotonica 2 		118 0 18 7.1E-02 0 0
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration 		195 0 23 7.0E-02 0 0
CUI: C0949664
Disease: Tauopathies
Tauopathies 		245 0 26 7.0E-02 0 0
CUI: C4302185
Disease: Atypical Parkinsonism
Atypical Parkinsonism 		30 0 12 6.9E-02 0 0
CUI: C0016667
Disease: Fragile X Syndrome
Fragile X Syndrome 		194 0 22 6.7E-02 0 0
CUI: C0005398
Disease: Cholestasis, Extrahepatic
Cholestasis, Extrahepatic 		87 0 15 6.6E-02 0 0
CUI: C0234119
Disease: Neuromuscular inhibition
Neuromuscular inhibition 		72 0 14 6.6E-02 0 0
CUI: C0342649
Disease: Vascular calcification
Vascular calcification 		257 0 25 6.5E-02 0 0
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations 		77 0 14 6.4E-02 0 0
CUI: C0410158
Disease: Muscle damage
Muscle damage 		163 0 19 6.4E-02 0 0
CUI: C0005859
Disease: Bloom Syndrome
Bloom Syndrome 		155 0 18 6.2E-02 0 0
CUI: C0338460
Disease: Argyrophilic grain disease
Argyrophilic grain disease 		18 0 10 6.1E-02 0 0
CUI: C0020437
Disease: Hypercalcemia
Hypercalcemia 		157 0 18 6.1E-02 0 0
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy 		176 0 19 6.1E-02 0 0
CUI: C1145628
Disease: Autonomic nervous system disorders
Autonomic nervous system disorders 		73 0 13 6.0E-02 0 0
CUI: C0410226
Disease: Congenital Myotonic Dystrophy
Congenital Myotonic Dystrophy 		9 0 9 5.8E-02 0 0
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		320 0 26 5.8E-02 0 0
CUI: C0520739
Disease: Hereditary pyropoikilocytosis
Hereditary pyropoikilocytosis 		47 0 11 5.8E-02 0 0
CUI: C0871189
Disease: Psychotic symptom
Psychotic symptom 		86 0 13 5.7E-02 0 0