Source: ALL
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: C0034139
Disease: Purine-Pyrimidine Metabolism, Inborn Errors
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
CUI: C2931781
Disease: Adenosine monophosphate deaminase deficiency
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
CUI: C4022546
Disease: Reduced erythrocyte 2,3-diphosphoglycerate concentration
Reduced erythrocyte 2,3-diphosphoglycerate concentration 		2 0 1 1.0E-01 0 0
CUI: C0033835
Disease: Pseudopseudohypoparathyroidism
Pseudopseudohypoparathyroidism 		14 0 2 9.5E-02 0 0
CUI: C0268147
Disease: Glycogen storage disease, type IX
Glycogen storage disease, type IX 		14 0 2 9.5E-02 0 0
CUI: C0004044
Disease: Asphyxia
Asphyxia 		3 0 1 9.1E-02 0 0
CUI: C0158242
Disease: Cervical spondylosis with myelopathy
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
CUI: C0268120
Disease: Adenine phosphoribosyltransferase deficiency
Adenine phosphoribosyltransferase deficiency 		3 0 1 9.1E-02 0 0
CUI: C0342245
Disease: Eye disorder due to diabetes mellitus
Eye disorder due to diabetes mellitus 		3 0 1 9.1E-02 0 0
CUI: C0342495
Disease: Macronodular adrenal hyperplasia
Macronodular adrenal hyperplasia 		15 0 2 9.1E-02 0 0
CUI: C0523631
Disease: Folic acid measurement
Folic acid measurement 		3 0 1 9.1E-02 0 0
CUI: C1265736
Disease: Orthokeratinized odontogenic cyst
Orthokeratinized odontogenic cyst 		3 0 1 9.1E-02 0 0
CUI: C1404521
Disease: Limb-girdle myopathy
Limb-girdle myopathy 		3 0 1 9.1E-02 0 0
CUI: C2931832
Disease: Hyperinsulinemic hypoglycemia, familial, 1
Hyperinsulinemic hypoglycemia, familial, 1 		3 0 1 9.1E-02 0 0
CUI: C2931833
Disease: Hyperinsulinemic hypoglycemia, familial, 2
Hyperinsulinemic hypoglycemia, familial, 2 		3 0 1 9.1E-02 0 0
CUI: C3179194
Disease: GALNS Deficiency
GALNS Deficiency 		3 0 1 9.1E-02 0 0
CUI: C4025714
Disease: Abnormality of the autonomic nervous system
Abnormality of the autonomic nervous system 		3 0 1 9.1E-02 0 0
CUI: C4524373
Disease: Hamster Melanoma
Hamster Melanoma 		3 0 1 9.1E-02 0 0