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: C0152190
Disease: Refractive amblyopia
Refractive amblyopia 		1 0 1 6.1E-03 0 0
CUI: C0152902
Disease: Tuberculosis of esophagus
Tuberculosis of esophagus 		1 0 1 6.1E-03 0 0
CUI: C0153053
Disease: Measles with complication
Measles with complication 		1 0 1 6.1E-03 0 0
CUI: C0153261
Disease: Histoplasma capsulatum Infection
Histoplasma capsulatum Infection 		1 0 1 6.1E-03 0 0
CUI: C0154565
Disease: Non-organic sleep disorder
Non-organic sleep disorder 		1 0 1 6.1E-03 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 6.1E-03 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 0 1 6.1E-03 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle 		1 0 1 6.1E-03 0 0
CUI: C0162164
Disease: Congenital stenosis of pulmonary valve
Congenital stenosis of pulmonary valve 		1 0 1 6.1E-03 0 0
CUI: C0206604
Disease: Arterivirus Infections
Arterivirus Infections 		1 0 1 6.1E-03 0 0
CUI: C0233594
Disease: Tail-biting
Tail-biting 		1 0 1 6.1E-03 0 0
CUI: C0234959
Disease: Panarteritis
Panarteritis 		1 0 1 6.1E-03 0 0
CUI: C0235267
Disease: Redness of eye
Redness of eye 		1 0 1 6.1E-03 0 0
CUI: C0235584
Disease: Granulocytopenia severe
Granulocytopenia severe 		1 0 1 6.1E-03 0 0
CUI: C0238518
Disease: Squamous cell carcinoma of vagina
Squamous cell carcinoma of vagina 		1 0 1 6.1E-03 0 0
CUI: C0239894
Disease: HEART DISPLACEMENT
HEART DISPLACEMENT 		1 0 1 6.1E-03 0 0
CUI: C0241518
Disease: Retraction of tympanic membrane
Retraction of tympanic membrane 		1 0 1 6.1E-03 0 0
CUI: C0262509
Disease: herpetic neuralgia
herpetic neuralgia 		1 0 1 6.1E-03 0 0
CUI: C0262981
Disease: Interface dermatitis
Interface dermatitis 		1 0 1 6.1E-03 0 0
CUI: C0263506
Disease: Perifolliculitis capitis abscedens
Perifolliculitis capitis abscedens 		1 0 1 6.1E-03 0 0
CUI: C0263579
Disease: Pigmented hairy epidermal nevus
Pigmented hairy epidermal nevus 		1 0 1 6.1E-03 0 0
CUI: C0265833
Disease: Congenital insufficiency of pulmonary valve
Congenital insufficiency of pulmonary valve 		1 0 1 6.1E-03 0 0
CUI: C0265978
Disease: Collagen nevus of skin
Collagen nevus of skin 		1 0 1 6.1E-03 0 0
CUI: C0267448
Disease: Eosinophilic colitis
Eosinophilic colitis 		1 0 1 6.1E-03 0 0
CUI: C0268461
Disease: Disorder of phenylalanine metabolism
Disorder of phenylalanine metabolism 		1 0 1 6.1E-03 0 0