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 4.1E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus
0 2 0 0 1 4.1E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 4.0E-03
CUI: C0268749
Disease: Fibrillary glomerulonephritis
Fibrillary glomerulonephritis
0 1 0 0 1 4.1E-03
CUI: C0268958
Disease: Acute orchitis
Acute orchitis
0 1 0 0 1 4.1E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 4.1E-03
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania
0 1 0 0 1 4.1E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 8.2E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 4.1E-03
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess
0 3 0 0 1 4.1E-03
DIABETES MELLITUS, INSULIN-DEPENDENT, SUSCEPTIBILITY TO
0 1 0 0 1 4.1E-03
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain
0 2 0 0 1 4.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 4.1E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 4.1E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 8.2E-03
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
219 0 1 1.4E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 1.4E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
169 0 1 1.5E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia
169 0 1 1.5E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression
165 0 1 1.5E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control
162 0 1 1.5E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior
135 0 1 1.6E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color
130 0 1 1.6E-03 0 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
130 0 1 1.6E-03 0 0
CUI: C0426429
Disease: Broad nasal tip
Broad nasal tip
125 0 1 1.6E-03 0 0