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: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
0 6385 0 0 1 1.6E-04
CUI: C0002390
Disease: Extrinsic allergic alveolitis
Extrinsic allergic alveolitis
1 0 1 3.3E-03 0 0
CUI: C0002624
Disease: Retrograde amnesia
Retrograde amnesia
1 0 1 3.3E-03 0 0
CUI: C0003090
Disease: Ankylosis
Ankylosis
1 0 1 3.3E-03 0 0
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia
1 0 1 3.3E-03 0 0
CUI: C0004698
Disease: Balkan Nephropathy
Balkan Nephropathy
1 0 1 3.3E-03 0 0
CUI: C0005683
Disease: Urinary Bladder Calculi (disorder)
Urinary Bladder Calculi (disorder)
1 0 1 3.3E-03 0 0
CUI: C0005694
Disease: Bladder neck obstruction
Bladder neck obstruction
1 0 1 3.3E-03 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis
1 0 1 3.3E-03 0 0
CUI: C0011057
Disease: Hearing Loss, Sudden
Hearing Loss, Sudden
1 0 1 3.3E-03 0 0
CUI: C0013930
Disease: Embolism, Tumor
Embolism, Tumor
1 0 1 3.3E-03 0 0
CUI: C0014866
Disease: Esophageal Stenosis
Esophageal Stenosis
1 0 1 3.3E-03 0 0
CUI: C0014869
Disease: Peptic Esophagitis
Peptic Esophagitis
1 0 1 3.3E-03 0 0
CUI: C0016325
Disease: Fluoride Poisoning
Fluoride Poisoning
1 0 1 3.3E-03 0 0
Hereditary fructose intolerance syndrome
1 0 1 3.3E-03 0 0
Fructose-1,6-Diphosphatase Deficiency
1 0 1 3.3E-03 0 0
CUI: C0017097
Disease: Gardner Syndrome
Gardner Syndrome
1 0 1 3.3E-03 0 0
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic
1 0 1 3.3E-03 0 0
Gerstmann-Straussler-Scheinker Disease
1 0 1 3.3E-03 0 0
CUI: C0017531
Disease: Angiolymphoid hyperplasia
Angiolymphoid hyperplasia
1 0 1 3.3E-03 0 0
CUI: C0018128
Disease: Graft Occlusion, Vascular
Graft Occlusion, Vascular
1 0 1 3.3E-03 0 0
CUI: C0018520
Disease: Halitosis
Halitosis
1 0 1 3.3E-03 0 0
CUI: C0018621
Disease: Hay fever
Hay fever
1 0 1 3.3E-03 0 0
CUI: C0018814
Disease: Heart Rupture, Post-Infarction
Heart Rupture, Post-Infarction
1 0 1 3.3E-03 0 0
CUI: C0019489
Disease: Deficiency, Hexosediphosphatase
Deficiency, Hexosediphosphatase
1 0 1 3.3E-03 0 0