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: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		0 4 0 0 1 5.0E-02
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		0 6 0 0 1 4.5E-02
CUI: C0201925
Disease: Calcium measurement
Calcium measurement 		0 71 0 0 1 1.1E-02
CUI: C0202100
Disease: Insulin C-peptide measurement
Insulin C-peptide measurement 		0 7 0 0 1 4.3E-02
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		0 2 0 0 1 5.6E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 5.9E-02
CUI: C0428302
Disease: Calcium level result
Calcium level result 		0 51 0 0 1 1.5E-02
CUI: C0728877
Disease: Serum albumin level
Serum albumin level 		0 9 0 0 1 4.0E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 0.12
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 5.6E-02
CUI: C3150714
Disease: FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5 		0 2 0 0 1 5.6E-02
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		187 0 1 1.6E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 1.7E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 1.7E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 1.7E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 1.7E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead 		149 0 1 1.7E-03 0 0
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		147 0 1 1.7E-03 0 0
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		147 0 1 1.7E-03 0 0
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		147 0 1 1.7E-03 0 0
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		131 0 1 1.8E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 1.8E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea 		129 0 1 1.8E-03 0 0
CUI: C0039075
Disease: Syndactyly
Syndactyly 		127 0 1 1.8E-03 0 0
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		124 243 1 1.8E-03 1 3.9E-03