Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Familial Alzheimer's disease of early onset
0 33 0 0 1 8.6E-03
CUI: C0002797
Disease: Bovine Anaplasmosis
Bovine Anaplasmosis
1 0 1 3.5E-03 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect
1 0 1 3.5E-03 0 0
CUI: C0003708
Disease: Arachnoiditis
Arachnoiditis
1 0 1 3.5E-03 0 0
CUI: C0006386
Disease: Bunion
Bunion
1 0 1 3.5E-03 0 0
CUI: C0006542
Disease: Byssinosis
Byssinosis
1 0 1 3.5E-03 0 0
CUI: C0007166
Disease: Low Cardiac Output
Low Cardiac Output
1 0 1 3.5E-03 0 0
CUI: C0008170
Disease: Chloramphenicol Resistance
Chloramphenicol Resistance
1 0 1 3.5E-03 0 0
CUI: C0009792
Disease: Consciousness Disorders
Consciousness Disorders
1 0 1 3.5E-03 0 0
CUI: C0010392
Disease: Crush syndrome
Crush syndrome
1 0 1 3.5E-03 0 0
CUI: C0016512
Disease: Foot pain
Foot pain
1 0 1 3.5E-03 0 0
CUI: C0019699
Disease: HIV Seropositivity
HIV Seropositivity
1 0 1 3.5E-03 0 0
CUI: C0027063
Disease: Myoclonic disorder
Myoclonic disorder
1 0 1 3.5E-03 0 0
CUI: C0027095
Disease: Myosarcoma
Myosarcoma
1 0 1 3.5E-03 0 0
Panniculitis, Nodular Nonsuppurative
1 0 1 3.5E-03 0 0
CUI: C0030925
Disease: Peptic Ulcer Perforation
Peptic Ulcer Perforation
1 0 1 3.5E-03 0 0
CUI: C0033075
Disease: Presbyopia
Presbyopia
1 0 1 3.5E-03 0 0
CUI: C0033247
Disease: Proctocolitis
Proctocolitis
1 0 1 3.5E-03 0 0
CUI: C0034350
Disease: Pyruvate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors
1 0 1 3.5E-03 0 0
CUI: C0037018
Disease: Shwartzman Phenomenon
Shwartzman Phenomenon
1 0 1 3.5E-03 0 0
CUI: C0085740
Disease: Mendelson Syndrome
Mendelson Syndrome
1 0 1 3.5E-03 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome
1 0 1 3.5E-03 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia
1 0 1 3.5E-03 0 0
Food poisoning caused by Vibrio parahaemolyticus
1 0 1 3.5E-03 0 0
CUI: C0153053
Disease: Measles with complication
Measles with complication
1 0 1 3.5E-03 0 0