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 2.9E-04
CUI: C0233689
Disease: Delusion of infidelity
Delusion of infidelity
0 1 0 0 1 2.9E-04
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 2.9E-04
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 1 2.9E-04
CUI: C0814144
Disease: endocrine system cancer
endocrine system cancer
0 1 0 0 1 2.9E-04
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 2 5.9E-04
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
0 1 0 0 1 2.9E-04
CORONARY ARTERY DISEASE, MODIFIER OF
0 1 0 0 1 2.9E-04
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
0 1 0 0 1 2.9E-04
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
0 1 0 0 1 2.9E-04
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome
0 1 0 0 1 2.9E-04
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 2.9E-04
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 2.9E-04
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO
0 1 0 0 1 2.9E-04
VASCULAR DEMENTIA, SUSCEPTIBILITY TO
0 1 0 0 1 2.9E-04
Frequent episodic tension-type headache
0 1 0 0 1 2.9E-04
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder)
20 0 1 1.4E-04 0 0
Abnormal isoelectric focusing of serum transferrin
15 0 1 1.4E-04 0 0
CUI: C4023786
Disease: Elevated levels of phytanic acid
Elevated levels of phytanic acid
15 0 1 1.4E-04 0 0
CUI: C1847164
Disease: Morning myoclonic jerks
Morning myoclonic jerks
11 0 1 1.4E-04 0 0
CUI: C1855675
Disease: Arima syndrome
Arima syndrome
11 0 1 1.4E-04 0 0
CUI: C2745997
Disease: OROFACIODIGITAL SYNDROME VI
OROFACIODIGITAL SYNDROME VI
11 0 1 1.4E-04 0 0
CUI: C4551571
Disease: Cranioectodermal dysplasia
Cranioectodermal dysplasia
11 0 1 1.4E-04 0 0
CUI: C4551856
Disease: Asphyxiating Thoracic Dystrophy 1
Asphyxiating Thoracic Dystrophy 1
11 0 1 1.4E-04 0 0
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER)
11 0 1 1.4E-04 0 0