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: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 8.0E-03
CUI: C0344535
Disease: Congenital corneal opacity
Congenital corneal opacity 		0 2 0 0 1 8.0E-03
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement 		58 0 1 1.1E-03 0 0
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		57 0 1 1.1E-03 0 0
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		54 0 1 1.1E-03 0 0
CUI: C1281901
Disease: Fatty acid measurement
Fatty acid measurement 		50 0 1 1.1E-03 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 1.1E-03 0 0
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		41 0 1 1.1E-03 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 1.1E-03 0 0
CUI: C3711376
Disease: Isodicentric Chromosome 15 Syndrome
Isodicentric Chromosome 15 Syndrome 		39 0 1 1.1E-03 0 0
CUI: C0742028
Disease: Cerebellar vermis atrophy
Cerebellar vermis atrophy 		32 0 1 1.1E-03 0 0
CUI: C1287365
Disease: Bilirubin level result
Bilirubin level result 		32 0 1 1.1E-03 0 0
CUI: C0019087
Disease: Hemorrhagic Disorders
Hemorrhagic Disorders 		30 0 1 1.1E-03 0 0
CUI: C0751362
Disease: Narcolepsy-Cataplexy Syndrome
Narcolepsy-Cataplexy Syndrome 		30 0 1 1.1E-03 0 0
CUI: C1266127
Disease: Histiocytoma, Angiomatoid Fibrous
Histiocytoma, Angiomatoid Fibrous 		28 0 1 1.1E-03 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome 		28 0 1 1.1E-03 0 0
CUI: C3158111
Disease: response to SSRI
response to SSRI 		28 0 1 1.1E-03 0 0
CUI: C0019025
Disease: Hemoglobin F Disease
Hemoglobin F Disease 		27 0 1 1.1E-03 0 0
CUI: C0019322
Disease: Umbilical hernia
Umbilical hernia 		27 0 1 1.1E-03 0 0
CUI: C0338430
Disease: Limbic Encephalitis
Limbic Encephalitis 		27 0 1 1.1E-03 0 0
CUI: C1855106
Disease: Neonatal onset
Neonatal onset 		27 0 1 1.1E-03 0 0
CUI: C1863416
Disease: Autosomal dominant compelling helio ophthalmic outburst syndrome
Autosomal dominant compelling helio ophthalmic outburst syndrome 		26 0 1 1.1E-03 0 0
CUI: C3898147
Disease: Neonatal Hypoxic Ischemic Encephalopathy
Neonatal Hypoxic Ischemic Encephalopathy 		26 0 1 1.1E-03 0 0
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome 		25 0 1 1.1E-03 0 0
CUI: C1318533
Disease: Secondary polycythemia
Secondary polycythemia 		25 0 1 1.1E-03 0 0