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 1.6E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus
0 2 0 0 1 1.6E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma
0 1 0 0 1 1.6E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 1.6E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 1.6E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 1.6E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 3.3E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 1 1.6E-03
Atrophia Maculosa Varioliformis Cutis, Familial
0 1 0 0 1 1.6E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 1.6E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 1.6E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.6E-03
VASCULAR DEMENTIA, SUSCEPTIBILITY TO
0 1 0 0 1 1.6E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 3.2E-03
CUI: C1836508
Disease: Generalized tonic seizures
Generalized tonic seizures
30 0 1 2.6E-04 0 0
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy
29 0 1 2.6E-04 0 0
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome
25 0 1 2.6E-04 0 0
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation
24 0 1 2.6E-04 0 0
Bone spicule pigmentation of the retina
24 0 1 2.6E-04 0 0
CUI: C4023683
Disease: EEG with spike-wave complexes
EEG with spike-wave complexes
23 0 1 2.6E-04 0 0
CUI: C1844945
Disease: Episodic respiratory distress
Episodic respiratory distress
21 0 1 2.6E-04 0 0
CUI: C3894553
Disease: response to simvastatin
response to simvastatin
21 0 1 2.6E-04 0 0
Renal dysplasia and retinal aplasia (disorder)
20 0 1 2.6E-04 0 0
CUI: C1845123
Disease: Generalized neonatal hypotonia
Generalized neonatal hypotonia
20 0 1 2.6E-04 0 0
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder)
20 0 1 2.6E-04 0 0