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 3.1E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus
0 2 0 0 1 3.0E-03
CUI: C0270639
Disease: Lateral Sinus Thrombosis
Lateral Sinus Thrombosis
0 1 0 0 1 3.1E-03
Heparin-induced thrombocytopenia with thrombosis
0 1 0 0 1 3.1E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 6.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 3.0E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 3.1E-03
CUI: C4722327
Disease: PROSTATE CANCER, HEREDITARY, 1
PROSTATE CANCER, HEREDITARY, 1
0 1 0 0 1 3.1E-03
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy
18 0 1 1.6E-04 0 0
CUI: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes
17 0 1 1.6E-04 0 0
CUI: C3658299
Disease: Zellweger Spectrum
Zellweger Spectrum
16 0 1 1.6E-04 0 0
Benign recurrent intrahepatic cholestasis
10 0 1 1.6E-04 0 0
CUI: C0342778
Disease: Ubiquinone dehydrogenase deficiency
Ubiquinone dehydrogenase deficiency
10 0 1 1.6E-04 0 0
CUI: C0432235
Disease: CRANIOECTODERMAL DYSPLASIA 1
CRANIOECTODERMAL DYSPLASIA 1
10 0 1 1.6E-04 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER
10 0 1 1.6E-04 0 0
CUI: C4551571
Disease: Cranioectodermal dysplasia
Cranioectodermal dysplasia
10 0 1 1.6E-04 0 0
CUI: C1852581
Disease: EPILEPSY, BENIGN NEONATAL, 2
EPILEPSY, BENIGN NEONATAL, 2
9 0 1 1.6E-04 0 0
Generalized Epilepsy with Febrile Seizures Plus
9 0 1 1.6E-04 0 0
CUI: C3889476
Disease: Benign Familial Convulsion
Benign Familial Convulsion
9 0 1 1.6E-04 0 0
Benign adult familial myoclonic epilepsy
9 0 1 1.6E-04 0 0
CUI: C0852975
Disease: Congenital cerebellar ataxia
Congenital cerebellar ataxia
8 0 1 1.6E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome
8 0 1 1.6E-04 0 0
CUI: C0175692
Disease: Johanson-Blizzard syndrome
Johanson-Blizzard syndrome
7 0 1 1.6E-04 0 0
CUI: C0265261
Disease: Multiple pterygium syndrome
Multiple pterygium syndrome
7 0 1 1.6E-04 0 0
CUI: C1850055
Disease: PEHO syndrome
PEHO syndrome
7 0 1 1.6E-04 0 0