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: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.5E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 1.5E-03
CUI: C0858353
Disease: Addicted to heroin
Addicted to heroin 		0 4 0 0 1 1.5E-03
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 1.5E-03
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 1.5E-03
CUI: C3178803
Disease: Social Anhedonia
Social Anhedonia 		0 4 0 0 1 1.5E-03
CUI: C3890602
Disease: Bodily Pain
Bodily Pain 		0 4 0 0 1 1.5E-03
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 1.5E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 1.6E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		156 0 1 1.6E-03 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion 		145 0 1 1.6E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 0 1 1.6E-03 0 0
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet 		129 0 1 1.7E-03 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth 		122 0 1 1.7E-03 0 0
CUI: C0576226
Disease: Short foot
Short foot 		116 0 1 1.7E-03 0 0
CUI: C0431447
Disease: Synophrys
Synophrys 		111 0 1 1.7E-03 0 0
CUI: C1843108
Disease: Short palm
Short palm 		110 0 1 1.7E-03 0 0
CUI: C0575802
Disease: Small hand
Small hand 		108 0 1 1.7E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		106 0 1 1.7E-03 0 0
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		105 0 1 1.7E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 1.7E-03 0 0
CUI: C0578038
Disease: Thin lips
Thin lips 		99 0 1 1.7E-03 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel 		96 0 1 1.7E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 1.7E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 1.8E-03 0 0