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: C0015702
Disease: Favism
Favism 		0 14 0 0 1 3.5E-03
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0 22 0 0 1 3.4E-03
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 1 3.3E-03
CUI: C0280252
Disease: stage, colon cancer
stage, colon cancer 		0 2 0 0 1 3.7E-03
CUI: C0523631
Disease: Folic acid measurement
Folic acid measurement 		0 8 0 0 1 3.6E-03
CUI: C1834750
Disease: CORONARY ARTERY DISEASE, MODIFIER OF
CORONARY ARTERY DISEASE, MODIFIER OF 		0 1 0 0 1 3.7E-03
CUI: C1834751
Disease: CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV 		0 1 0 0 1 3.7E-03
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		0 33 0 0 1 3.3E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 3.7E-03
CUI: C4024948
Disease: Anterior encephalocele
Anterior encephalocele 		0 5 0 0 1 3.7E-03
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		338 456 1 1.9E-03 1 1.4E-03
CUI: C1314691
Disease: Age at menarche
Age at menarche 		267 0 1 2.2E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		261 0 1 2.2E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 2.4E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 2.5E-03 0 0
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		192 0 1 2.6E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 2.6E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 2.8E-03 0 0
CUI: C4025790
Disease: Specific learning disability
Specific learning disability 		165 0 1 2.8E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers 		160 0 1 2.8E-03 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 0 1 2.8E-03 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism 		148 0 1 2.9E-03 0 0
CUI: C4551485
Disease: Clinodactyly
Clinodactyly 		148 0 1 2.9E-03 0 0
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		146 0 1 2.9E-03 0 0
CUI: C1879321
Disease: Acute Myeloid Leukemia (AML-M2)
Acute Myeloid Leukemia (AML-M2) 		143 0 1 3.0E-03 0 0