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: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		223 0 1 2.0E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 2.0E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.2E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.2E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 2.3E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		156 0 1 2.3E-03 0 0
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		147 0 1 2.3E-03 0 0
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		147 0 1 2.3E-03 0 0
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		147 0 1 2.3E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 1 2.3E-03 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		137 0 1 2.4E-03 0 0
CUI: C0576226
Disease: Short foot
Short foot 		116 0 1 2.5E-03 0 0
CUI: C0221629
Disease: Proximal muscle weakness
Proximal muscle weakness 		112 0 1 2.5E-03 0 0
CUI: C0575802
Disease: Small hand
Small hand 		108 0 1 2.5E-03 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 2.5E-03 0 0
CUI: C1853246
Disease: Eversion of lower lip
Eversion of lower lip 		105 0 1 2.6E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 2.6E-03 0 0
CUI: C1837142
Disease: Poor suck
Poor suck 		103 0 1 2.6E-03 0 0
CUI: C0282577
Disease: Congenital Disorders of Glycosylation
Congenital Disorders of Glycosylation 		102 0 1 2.6E-03 0 0
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples 		96 0 1 2.6E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 2.6E-03 0 0
CUI: C0850703
Disease: Frequent falls
Frequent falls 		94 0 1 2.6E-03 0 0
CUI: C1263857
Disease: Peripheral axonal neuropathy
Peripheral axonal neuropathy 		94 0 1 2.6E-03 0 0
CUI: C0020626
Disease: Hypoparathyroidism
Hypoparathyroidism 		92 0 1 2.6E-03 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers 		92 0 1 2.6E-03 0 0