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: C0009398
Disease: Color vision defect
Color vision defect
0 4 0 0 2 2.8E-03
CUI: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic
0 1 0 0 1 1.4E-03
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 1 0 0 1 1.4E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.4E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus
0 2 0 0 1 1.4E-03
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia
0 4 0 0 1 1.4E-03
CUI: C0264411
Disease: Hay fever with asthma
Hay fever with asthma
0 1 0 0 1 1.4E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 2 0 0 1 1.4E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis
0 1 0 0 1 1.4E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 2.8E-03
Severe nonproliferative diabetic retinopathy
0 3 0 0 1 1.4E-03
CUI: C0860602
Disease: Anxious personality
Anxious personality
0 2 0 0 1 1.4E-03
CUI: C0865791
Disease: Obstructive bronchitis
Obstructive bronchitis
0 1 0 0 1 1.4E-03
CUI: C1275149
Disease: Multiple skin tags
Multiple skin tags
0 1 0 0 1 1.4E-03
Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant
0 2 0 0 2 2.8E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.4E-03
CUI: C0000729
Disease: Abdominal Cramps
Abdominal Cramps
1 0 1 5.8E-04 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis
1 0 1 5.8E-04 0 0
CUI: C0001529
Disease: Adiposis Dolorosa
Adiposis Dolorosa
1 0 1 5.8E-04 0 0
CUI: C0002625
Disease: Amnestic Disorder
Amnestic Disorder
1 0 1 5.8E-04 0 0
CUI: C0002631
Disease: Infection of amniotic cavity
Infection of amniotic cavity
1 0 1 5.8E-04 0 0
CUI: C0002831
Disease: Ancylostomiasis
Ancylostomiasis
1 0 1 5.8E-04 0 0
CUI: C0003510
Disease: Aortitis Syndrome
Aortitis Syndrome
1 0 1 5.8E-04 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect
1 0 1 5.8E-04 0 0
CUI: C0003564
Disease: Aphonia
Aphonia
1 0 1 5.8E-04 0 0