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: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 13 0.65 0 0
CUI: C1847720
Disease: Hypermethioninemia due to deficiency of glycine N-methyltransferase
Hypermethioninemia due to deficiency of glycine N-methyltransferase 		3 0 2 0.14 0 0
CUI: C3151058
Disease: S-adenosylhomocysteine hydrolase deficiency
S-adenosylhomocysteine hydrolase deficiency 		3 0 2 0.14 0 0
CUI: C0268528
Disease: Hyperprolinemia
Hyperprolinemia 		4 0 2 0.13 0 0
CUI: C0268128
Disease: Orotic aciduria
Orotic aciduria 		6 0 2 0.12 0 0
CUI: C0340848
Disease: PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE
PULMONARY VENOOCCLUSIVE DISEASE 2, AUTOSOMAL RECESSIVE 		1 0 1 7.7E-02 0 0
CUI: C0431603
Disease: Ectopic liver
Ectopic liver 		1 0 1 7.7E-02 0 0
CUI: C0523852
Disease: Proline measurement
Proline measurement 		1 0 1 7.7E-02 0 0
CUI: C0598675
Disease: inborn aminoaciduria
inborn aminoaciduria 		1 0 1 7.7E-02 0 0
CUI: C0856208
Disease: Increased serum zinc
Increased serum zinc 		1 0 1 7.7E-02 0 0
CUI: C1291463
Disease: Deficiency of phosphoserine phosphatase
Deficiency of phosphoserine phosphatase 		1 0 1 7.7E-02 0 0
CUI: C1833247
Disease: SCHIZOPHRENIA 4 (disorder)
SCHIZOPHRENIA 4 (disorder) 		1 0 1 7.7E-02 0 0
CUI: C1856603
Disease: Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to
Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia due to 		1 0 1 7.7E-02 0 0
CUI: C1856604
Disease: Late-onset spinocerebellar degeneration
Late-onset spinocerebellar degeneration 		1 0 1 7.7E-02 0 0
CUI: C3698354
Disease: Pulmonary veno-occlusive disease and/or pulmonary capillary hemangiomatosis
Pulmonary veno-occlusive disease and/or pulmonary capillary hemangiomatosis 		1 0 1 7.7E-02 0 0
CUI: C4020753
Disease: Intimal fibrosis
Intimal fibrosis 		1 0 1 7.7E-02 0 0
CUI: C4021106
Disease: Elevated coagulation factor V activity
Elevated coagulation factor V activity 		1 0 1 7.7E-02 0 0
CUI: C4024698
Disease: Diaminoaciduria
Diaminoaciduria 		1 0 1 7.7E-02 0 0
CUI: C4510276
Disease: Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency 		1 0 1 7.7E-02 0 0
CUI: C0268621
Disease: Hepatic methionine adenosyltransferase deficiency
Hepatic methionine adenosyltransferase deficiency 		16 0 2 7.4E-02 0 0
CUI: C4048705
Disease: Hypermethioninemia
Hypermethioninemia 		16 0 2 7.4E-02 0 0
CUI: C0010074
Disease: Coronary Vessel Anomalies
Coronary Vessel Anomalies 		2 0 1 7.1E-02 0 0
CUI: C0018500
Disease: Hair Diseases
Hair Diseases 		17 0 2 7.1E-02 0 0
CUI: C0018949
Disease: Hematomyelia
Hematomyelia 		2 0 1 7.1E-02 0 0
CUI: C0021833
Disease: Intestinal Fistula
Intestinal Fistula 		2 0 1 7.1E-02 0 0