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: C0268121
Disease: APRT deficiency, Japanese type
APRT deficiency, Japanese type
1 0 1 0.11 0 0
Hyperinsulinemic hypoglycemia, familial, 3
1 0 1 0.11 0 0
Epidermal growth factor receptor negative non-small cell lung cancer
1 0 1 0.11 0 0
CUI: C2609269
Disease: Fasting hyperglycaemia
Fasting hyperglycaemia
1 0 1 0.11 0 0
Erythrocyte Amp Deaminase Deficiency
1 0 1 0.11 0 0
DIABETES MELLITUS, NONINSULIN-DEPENDENT, LATE-ONSET
1 0 1 0.11 0 0
CUI: C4017156
Disease: MCARDLE DISEASE, MILD
MCARDLE DISEASE, MILD
1 0 1 0.11 0 0
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 59
1 0 1 0.11 0 0
CUI: C0010074
Disease: Coronary Vessel Anomalies
Coronary Vessel Anomalies
2 0 1 1.0E-01 0 0
Purine-Pyrimidine Metabolism, Inborn Errors
2 0 1 1.0E-01 0 0
CUI: C0151465
Disease: Renal abscess
Renal abscess
2 0 1 1.0E-01 0 0
CUI: C0271702
Disease: Iatrogenic hyperinsulinism
Iatrogenic hyperinsulinism
2 0 1 1.0E-01 0 0
CUI: C0302872
Disease: MYELOMA, ENDOTHELIAL
MYELOMA, ENDOTHELIAL
2 0 1 1.0E-01 0 0
CUI: C0749557
Disease: toe necrosis
toe necrosis
2 0 1 1.0E-01 0 0
CUI: C0751692
Disease: Multiple Hemangioblastomas
Multiple Hemangioblastomas
2 0 1 1.0E-01 0 0
Adenosine monophosphate deaminase deficiency
2 0 1 1.0E-01 0 0
CUI: C3203622
Disease: Crystal nephropathy
Crystal nephropathy
2 0 1 1.0E-01 0 0
Reduced erythrocyte 2,3-diphosphoglycerate concentration
2 0 1 1.0E-01 0 0
CUI: C0004044
Disease: Asphyxia
Asphyxia
3 0 1 9.1E-02 0 0
CUI: C0151236
Disease: Conduction system abnormalities
Conduction system abnormalities
3 0 2 0.20 0 0
Cervical spondylosis with myelopathy
3 0 1 9.1E-02 0 0
CUI: C0268117
Disease: Gout, HPRT-Related
Gout, HPRT-Related
3 0 1 9.1E-02 0 0
Adenine phosphoribosyltransferase deficiency
3 0 1 9.1E-02 0 0
CUI: C0340420
Disease: Cardiac glycogenosis
Cardiac glycogenosis
3 0 2 0.20 0 0
Eye disorder due to diabetes mellitus
3 0 1 9.1E-02 0 0