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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic
0 1 0 0 1 8.1E-03
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 7.6E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 8.1E-03
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis
0 1 0 0 1 8.1E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 1.6E-02
CUI: C0752138
Disease: Intracranial Arterial Diseases
Intracranial Arterial Diseases
0 1 0 0 1 8.1E-03
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess
0 3 0 0 1 8.0E-03
CORONARY ARTERY DISEASE, MODIFIER OF
0 1 0 0 1 8.1E-03
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
0 1 0 0 1 8.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 8.0E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 8.1E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO
0 1 0 0 1 8.1E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 1.6E-02
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia
118 0 1 1.2E-03 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness
87 0 1 1.3E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea
82 0 1 1.3E-03 0 0
CUI: C1839630
Disease: Severe muscular hypotonia
Severe muscular hypotonia
75 0 1 1.3E-03 0 0
CUI: C0240538
Disease: Convex nasal ridge
Convex nasal ridge
69 0 1 1.3E-03 0 0
CUI: C1261430
Disease: Fasting blood sugar result
Fasting blood sugar result
65 0 1 1.3E-03 0 0
CUI: C0156394
Disease: Hypertrophy of clitoris
Hypertrophy of clitoris
63 0 1 1.3E-03 0 0
CUI: C0004144
Disease: Atelectasis
Atelectasis
62 0 1 1.3E-03 0 0
CUI: C0234378
Disease: Static Tremor
Static Tremor
62 0 1 1.3E-03 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function
59 0 1 1.3E-03 0 0
CUI: C0338502
Disease: Hypoplasia of the optic nerve
Hypoplasia of the optic nerve
59 0 1 1.3E-03 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
58 0 1 1.3E-03 0 0