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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.1E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 3.1E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 3.1E-03
CUI: C0278252
Disease: Prognosis bad
Prognosis bad 		0 2 0 0 1 3.1E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE 		0 1 0 0 1 3.1E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 3.1E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 3.1E-03
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 6.1E-03
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 3.1E-03
CUI: C1300256
Disease: Thanatophoric dysplasia, type 1
Thanatophoric dysplasia, type 1 		0 4 0 0 1 3.0E-03
CUI: C2699063
Disease: Resistin Measurement
Resistin Measurement 		0 6 0 0 1 3.0E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 3.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 3.0E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.1E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 3.1E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 6.1E-03
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 1 6.1E-04 0 0
CUI: C0239067
Disease: Difficulty walking up stairs
Difficulty walking up stairs 		51 0 1 6.1E-04 0 0
CUI: C1843700
Disease: Increased variability in muscle fiber diameter
Increased variability in muscle fiber diameter 		50 0 1 6.1E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 6.1E-04 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 1 6.1E-04 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 6.1E-04 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 6.1E-04 0 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate 		45 0 1 6.1E-04 0 0
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness 		44 0 1 6.1E-04 0 0