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 8.9E-03
CUI: C0233689
Disease: Delusion of infidelity
Delusion of infidelity
0 1 0 0 1 8.9E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 8.9E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder)
0 1 0 0 1 8.9E-03
CUI: C0745031
Disease: homicidal
homicidal
0 2 0 0 1 8.8E-03
SPINAL MUSCULAR ATROPHY, LATE-ONSET, FINKEL TYPE
0 1 0 0 1 8.9E-03
AMYOTROPHIC LATERAL SCLEROSIS, TYPICAL
0 1 0 0 1 8.9E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder)
0 1 0 0 1 8.9E-03
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant
0 1 0 0 1 8.9E-03
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome
0 1 0 0 1 8.9E-03
CUI: C2678503
Disease: AXENFELD-RIEGER SYNDROME, TYPE 3
AXENFELD-RIEGER SYNDROME, TYPE 3
0 27 0 0 2 1.5E-02
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6
0 1 0 0 1 8.9E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 8.8E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 8.9E-03
Frequent episodic tension-type headache
0 1 0 0 1 8.9E-03
CUI: C0000727
Disease: Abdomen, Acute
Abdomen, Acute
2 0 1 7.9E-04 0 0
CUI: C0000887
Disease: Acantholysis
Acantholysis
11 0 1 7.9E-04 0 0
CUI: C0001075
Disease: Achlorhydria
Achlorhydria
5 0 1 7.9E-04 0 0
CUI: C0001197
Disease: Acrodermatitis
Acrodermatitis
5 0 1 7.9E-04 0 0
CUI: C0001202
Disease: Acrokeratosis
Acrokeratosis
3 0 1 7.9E-04 0 0
CUI: C0001261
Disease: Actinomycosis
Actinomycosis
1 0 1 7.9E-04 0 0
Acute and subacute liver necrosis (disorder)
6 0 1 7.9E-04 0 0
Herpetic Acute Necrotizing Encephalitis
5 0 1 7.9E-04 0 0
CUI: C0001433
Disease: Adenoma, Acidophil
Adenoma, Acidophil
2 0 1 7.9E-04 0 0
Adjustment disorder with depressed mood
1 0 1 7.9E-04 0 0