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: C3150862
Disease: HEMOCHROMATOSIS, JUVENILE, DIGENIC
HEMOCHROMATOSIS, JUVENILE, DIGENIC 		0 1 0 0 1 7.1E-03
CUI: C3280096
Disease: TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2
TRANSFERRIN SERUM LEVEL QUANTITATIVE TRAIT LOCUS 2 		0 2 0 0 1 7.0E-03
CUI: C3280647
Disease: BACTEREMIA, SUSCEPTIBILITY TO, 2
BACTEREMIA, SUSCEPTIBILITY TO, 2 		0 1 0 0 1 7.1E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 7.1E-03
CUI: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia 		0 23 0 0 1 6.1E-03
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 7.3E-04 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology 		70 0 1 7.4E-04 0 0
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		67 108 1 7.4E-04 1 4.0E-03
CUI: C0156394
Disease: Hypertrophy of clitoris
Hypertrophy of clitoris 		63 0 1 7.4E-04 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 1 7.4E-04 0 0
CUI: C0263523
Disease: Micronychia (disorder)
Micronychia (disorder) 		60 0 1 7.4E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 7.4E-04 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 7.5E-04 0 0
CUI: C0432103
Disease: Submucous cleft of hard palate
Submucous cleft of hard palate 		55 0 1 7.5E-04 0 0
CUI: C1278049
Disease: Serum gamma-glutamyl transferase measurement
Serum gamma-glutamyl transferase measurement 		54 0 1 7.5E-04 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		50 0 1 7.5E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 7.5E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 7.5E-04 0 0
CUI: C1837731
Disease: Overfolded helix
Overfolded helix 		46 0 1 7.5E-04 0 0
CUI: C2112129
Disease: Postaxial foot polydactyly
Postaxial foot polydactyly 		45 0 1 7.5E-04 0 0
CUI: C0546967
Disease: Posterior embryotoxon
Posterior embryotoxon 		44 0 1 7.5E-04 0 0
CUI: C1866190
Disease: Atresia of the external auditory canal
Atresia of the external auditory canal 		44 0 1 7.5E-04 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		42 0 1 7.5E-04 0 0
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		41 259 1 7.5E-04 1 2.5E-03
CUI: C0266631
Disease: Accessory spleen
Accessory spleen 		41 0 1 7.5E-04 0 0