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: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		90 0 1 3.0E-03 0 0
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		89 0 1 3.0E-03 0 0
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		89 0 1 3.0E-03 0 0
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		88 0 1 3.0E-03 0 0
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		88 0 1 3.0E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 3.0E-03 0 0
CUI: C0750937
Disease: Ataxia, Appendicular
Ataxia, Appendicular 		86 0 1 3.0E-03 0 0
CUI: C4021813
Disease: Oral cleft
Oral cleft 		85 0 1 3.0E-03 0 0
CUI: C4521256
Disease: Glomerulopathy Assessment
Glomerulopathy Assessment 		84 0 1 3.1E-03 0 0
CUI: C0339527
Disease: Leber Congenital Amaurosis
Leber Congenital Amaurosis 		83 0 1 3.1E-03 0 0
CUI: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		83 0 1 3.1E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 3.1E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 3.1E-03 0 0
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		82 0 1 3.1E-03 0 0
CUI: C0020758
Disease: Congenital ichthyosis
Congenital ichthyosis 		80 0 1 3.1E-03 0 0
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		80 0 1 3.1E-03 0 0
CUI: C1834405
Disease: Nail dysplasia
Nail dysplasia 		78 0 1 3.1E-03 0 0
CUI: C1843156
Disease: Progressive sensorineural hearing impairment
Progressive sensorineural hearing impairment 		78 0 1 3.1E-03 0 0
CUI: C4321245
Disease: Cleft lip or lips
Cleft lip or lips 		78 0 1 3.1E-03 0 0
CUI: C0221210
Disease: Congenital malrotation of intestine
Congenital malrotation of intestine 		77 0 1 3.1E-03 0 0
CUI: C0423757
Disease: Thin skin
Thin skin 		77 0 1 3.1E-03 0 0
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
Lower Urinary Tract Symptoms 		77 0 1 3.1E-03 0 0
CUI: C3279947
Disease: NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9
NAIL DISORDER, NONSYNDROMIC CONGENITAL, 9 		77 0 1 3.1E-03 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2 		76 0 1 3.1E-03 0 0
CUI: C0009676
Disease: Confusion
Confusion 		75 0 1 3.1E-03 0 0