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: C4049262
Disease: Febrile infection related epilepsy syndrome
Febrile infection related epilepsy syndrome 		8 0 3 0.15 0 0
CUI: C0242993
Disease: Nephropathia Epidemica
Nephropathia Epidemica 		9 0 3 0.14 0 0
CUI: C0340291
Disease: Silent myocardial ischemia
Silent myocardial ischemia 		9 0 3 0.14 0 0
CUI: C3280062
Disease: LEBER CONGENITAL AMAUROSIS 16
LEBER CONGENITAL AMAUROSIS 16 		2 0 2 0.13 0 0
CUI: C4073118
Disease: Optically empty vitreous
Optically empty vitreous 		2 0 2 0.13 0 0
CUI: C0155366
Disease: Vitreous degeneration
Vitreous degeneration 		3 1 2 0.12 1 1.00
CUI: C2748507
Disease: INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY
INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY 		3 0 2 0.12 0 0
CUI: C0152087
Disease: Crystal Arthropathies
Crystal Arthropathies 		4 0 2 0.12 0 0
CUI: C4749462
Disease: New-onset refractory status epilepticus
New-onset refractory status epilepticus 		4 0 2 0.12 0 0
CUI: C0153257
Disease: Primary pulmonary coccidioidomycosis
Primary pulmonary coccidioidomycosis 		5 0 2 0.11 0 0
CUI: C0403528
Disease: Henoch-Schönlein nephritis
Henoch-Schönlein nephritis 		5 0 2 0.11 0 0
CUI: C0521626
Disease: Fibrosis of urinary bladder
Fibrosis of urinary bladder 		5 0 2 0.11 0 0
CUI: C3826476
Disease: Dental caries in children
Dental caries in children 		6 0 2 0.11 0 0
CUI: C0376300
Disease: Dengue Shock Syndrome
Dengue Shock Syndrome 		18 0 3 1.0E-01 0 0
CUI: C1838577
Disease: Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy 		7 0 2 1.0E-01 0 0
CUI: C1840452
Disease: Hyaloideoretinal degeneration of Wagner
Hyaloideoretinal degeneration of Wagner 		7 0 2 1.0E-01 0 0
CUI: C0030804
Disease: Pemphigoid, Benign Mucous Membrane
Pemphigoid, Benign Mucous Membrane 		19 0 3 9.7E-02 0 0
CUI: C1290638
Disease: Resorption of apex of tooth root
Resorption of apex of tooth root 		8 0 2 9.5E-02 0 0
CUI: C4082167
Disease: Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis Syndrome
Periodic Fever, Aphthous Stomatitis, Pharyngitis, Adenitis Syndrome 		8 0 2 9.5E-02 0 0
CUI: C4551861
Disease: Telangiectasia, Hereditary Hemorrhagic, Type 1
Telangiectasia, Hereditary Hemorrhagic, Type 1 		8 0 2 9.5E-02 0 0
CUI: C0344290
Disease: Vitreoretinal degeneration
Vitreoretinal degeneration 		20 6 3 9.4E-02 1 0.17
CUI: C4552003
Disease: EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1
EHLERS-DANLOS SYNDROME, SPONDYLODYSPLASTIC TYPE, 1 		9 0 2 9.1E-02 0 0
CUI: C0795996
Disease: STRIATONIGRAL DEGENERATION, INFANTILE (disorder)
STRIATONIGRAL DEGENERATION, INFANTILE (disorder) 		10 0 2 8.7E-02 0 0
CUI: C1456399
Disease: Crushing sensation
Crushing sensation 		10 0 2 8.7E-02 0 0
CUI: C4543758
Disease: Protracted bronchitis caused by bacterium
Protracted bronchitis caused by bacterium 		10 0 2 8.7E-02 0 0