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: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		0 11 0 0 1 6.3E-03
CUI: C0017741
Disease: Glucose tolerance test
Glucose tolerance test 		0 28 0 0 1 5.6E-03
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		0 6 0 0 1 6.5E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 6.6E-03
CUI: C0201874
Disease: Amino acids measurement
Amino acids measurement 		0 92 0 0 1 4.1E-03
CUI: C0202100
Disease: Insulin C-peptide measurement
Insulin C-peptide measurement 		0 7 0 0 1 6.4E-03
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		0 2 0 0 1 6.6E-03
CUI: C0342942
Disease: Generalized obesity
Generalized obesity 		0 4 0 0 1 6.5E-03
CUI: C0728877
Disease: Serum albumin level
Serum albumin level 		0 9 0 0 1 6.3E-03
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 1 6.6E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 6.6E-03
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		0 108 0 0 1 3.9E-03
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0 134 0 0 1 3.5E-03
CUI: C1834750
Disease: CORONARY ARTERY DISEASE, MODIFIER OF
CORONARY ARTERY DISEASE, MODIFIER OF 		0 1 0 0 1 6.7E-03
CUI: C1834751
Disease: CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV 		0 1 0 0 1 6.7E-03
CUI: C2825856
Disease: Factor VII measurement
Factor VII measurement 		0 36 0 0 1 5.4E-03
CUI: C3150714
Disease: FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5 		0 2 0 0 1 6.6E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 6.7E-03
CUI: C0311394
Disease: Difficulty walking
Difficulty walking 		224 0 1 1.7E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 1.8E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 1.9E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 1.9E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 1.9E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 0 1 2.0E-03 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow 		141 0 1 2.0E-03 0 0