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: C1843244
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 		0 10 0 0 1 1.5E-02
CUI: C1849043
Disease: Soft, doughy skin
Soft, doughy skin 		0 4 0 0 1 1.7E-02
CUI: C1859481
Disease: Abnormal finger flexion creases
Abnormal finger flexion creases 		0 1 0 0 1 1.8E-02
CUI: C1969810
Disease: FEBRILE CONVULSIONS, FAMILIAL, 8
FEBRILE CONVULSIONS, FAMILIAL, 8 		0 13 0 0 1 1.4E-02
CUI: C4021603
Disease: Widely spaced primary teeth
Widely spaced primary teeth 		0 1 0 0 1 1.8E-02
CUI: C4024661
Disease: Abnormality of the vertebral spinous processes
Abnormality of the vertebral spinous processes 		0 1 0 0 1 1.8E-02
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 1.8E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 2.0E-03 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 1 2.0E-03 0 0
CUI: C0013575
Disease: Ectodermal Dysplasia
Ectodermal Dysplasia 		71 0 1 2.0E-03 0 0
CUI: C0276275
Disease: Disease due to Parvoviridae
Disease due to Parvoviridae 		71 0 1 2.0E-03 0 0
CUI: C1844383
Disease: Recurrent bacterial infection
Recurrent bacterial infection 		69 0 1 2.0E-03 0 0
CUI: C0562350
Disease: Hip circumference
Hip circumference 		68 0 1 2.0E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 2.0E-03 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result 		65 0 1 2.0E-03 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 2.1E-03 0 0
CUI: C0238013
Disease: Invasive aspergillosis
Invasive aspergillosis 		59 0 1 2.1E-03 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 2.1E-03 0 0
CUI: C0016514
Disease: Foot-and-Mouth Disease
Foot-and-Mouth Disease 		56 0 1 2.1E-03 0 0
CUI: C0869220
Disease: Adverse effects, not elsewhere classified
Adverse effects, not elsewhere classified 		55 0 1 2.1E-03 0 0
CUI: C0008372
Disease: Intrahepatic Cholestasis
Intrahepatic Cholestasis 		54 0 1 2.1E-03 0 0
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		54 0 1 2.1E-03 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 8 1 2.1E-03 1 1.6E-02
CUI: C0699743
Disease: Congenital muscular dystrophy (disorder)
Congenital muscular dystrophy (disorder) 		54 0 1 2.1E-03 0 0
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		54 0 1 2.1E-03 0 0