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: C0576227
Disease: Narrow foot
Narrow foot 		6 0 1 0.17 0 0
CUI: C1970827
Disease: Phosphoribosylpyrophosphate Synthetase Superactivity
Phosphoribosylpyrophosphate Synthetase Superactivity 		6 0 1 0.17 0 0
CUI: C1971021
Disease: Potassium depletion
Potassium depletion 		6 0 1 0.17 0 0
CUI: C2349595
Disease: Fetal anemia
Fetal anemia 		6 0 1 0.17 0 0
CUI: C4022737
Disease: Neurodevelopmental abnormality
Neurodevelopmental abnormality 		7 19 1 0.14 1 4.8E-02
CUI: C0242073
Disease: Pulmonary congestion
Pulmonary congestion 		10 0 1 1.0E-01 0 0
CUI: C4021765
Disease: Morphological abnormality of the central nervous system
Morphological abnormality of the central nervous system 		10 7 1 1.0E-01 1 0.11
CUI: C0268119
Disease: Combined molybdoflavoprotein enzyme deficiency
Combined molybdoflavoprotein enzyme deficiency 		13 0 1 7.7E-02 0 0
CUI: C1853230
Disease: Aphakia, congenital primary
Aphakia, congenital primary 		14 0 1 7.1E-02 0 0
CUI: C3805083
Disease: Portal fibrosis
Portal fibrosis 		15 0 1 6.7E-02 0 0
CUI: C0268621
Disease: Hepatic methionine adenosyltransferase deficiency
Hepatic methionine adenosyltransferase deficiency 		16 0 1 6.2E-02 0 0
CUI: C4048705
Disease: Hypermethioninemia
Hypermethioninemia 		16 0 1 6.2E-02 0 0
CUI: C0268124
Disease: Adenosine deaminase deficiency
Adenosine deaminase deficiency 		17 0 1 5.9E-02 0 0
CUI: C2930868
Disease: Rasmussen subacute encephalitis
Rasmussen subacute encephalitis 		17 0 1 5.9E-02 0 0
CUI: C0393484
Disease: Rasmussen Syndrome
Rasmussen Syndrome 		18 0 1 5.6E-02 0 0
CUI: C0392607
Disease: Severe combined immunodeficiency due to adenosine deaminase deficiency
Severe combined immunodeficiency due to adenosine deaminase deficiency 		24 0 1 4.2E-02 0 0
CUI: C0003129
Disease: Anoxemia
Anoxemia 		33 0 1 3.0E-02 0 0
CUI: C0010403
Disease: Cryoglobulinemia
Cryoglobulinemia 		37 0 1 2.7E-02 0 0
CUI: C0748607
Disease: Recurrent seizure
Recurrent seizure 		44 0 1 2.3E-02 0 0
CUI: C0205646
Disease: Adenoma, Basal Cell
Adenoma, Basal Cell 		49 0 1 2.0E-02 0 0
CUI: C0700292
Disease: Hypoxemia
Hypoxemia 		52 0 1 1.9E-02 0 0
CUI: C0232744
Disease: Decreased liver function
Decreased liver function 		59 0 1 1.7E-02 0 0
CUI: C0242184
Disease: Hypoxia
Hypoxia 		59 0 1 1.7E-02 0 0
CUI: C0206685
Disease: Acinar Cell Carcinoma
Acinar Cell Carcinoma 		65 0 1 1.5E-02 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver 		75 8 1 1.3E-02 1 1.0E-01