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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 3.9E-04
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 1 3.8E-04
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 3.9E-04
CUI: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance 		0 1 0 0 1 3.9E-04
CUI: C0523354
Disease: Complement factor I measurement
Complement factor I measurement 		0 1 0 0 1 3.9E-04
CUI: C0747198
Disease: pancreatitis idiopathic
pancreatitis idiopathic 		0 4 0 0 1 3.9E-04
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		105 0 1 7.9E-04 0 0
CUI: C1849265
Disease: Overgrowth
Overgrowth 		103 0 1 7.9E-04 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc 		98 0 1 8.0E-04 0 0
CUI: C1720983
Disease: Channelopathies
Channelopathies 		94 0 1 8.0E-04 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 8.1E-04 0 0
CUI: C1855728
Disease: Low posterior hairline
Low posterior hairline 		86 0 1 8.1E-04 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 0 1 8.1E-04 0 0
CUI: C1853738
Disease: Long eyelashes
Long eyelashes 		83 0 1 8.1E-04 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 8.1E-04 0 0
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		80 0 1 8.1E-04 0 0
CUI: C1737329
Disease: Dysmorphism
Dysmorphism 		80 0 1 8.1E-04 0 0
CUI: C0004930
Disease: Behavior Disorders
Behavior Disorders 		77 0 1 8.1E-04 0 0
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
Lower Urinary Tract Symptoms 		77 0 1 8.1E-04 0 0
CUI: C1836296
Disease: Muscle Weakness Lower Limb
Muscle Weakness Lower Limb 		74 0 1 8.1E-04 0 0
CUI: C0521620
Disease: Dilatation of ureter
Dilatation of ureter 		72 0 1 8.1E-04 0 0
CUI: C1842366
Disease: Low anterior hairline
Low anterior hairline 		71 0 1 8.2E-04 0 0
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly 		67 0 1 8.2E-04 0 0
CUI: C0268237
Disease: Cytochrome-c Oxidase Deficiency
Cytochrome-c Oxidase Deficiency 		65 0 1 8.2E-04 0 0
CUI: C0376705
Disease: Viral Load result
Viral Load result 		65 0 1 8.2E-04 0 0