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: C0948585
Disease: Hydroxyprolinuria
Hydroxyprolinuria 		8 0 5 0.56 0 0
CUI: C0268654
Disease: Iminoglycinuria
Iminoglycinuria 		4 0 3 0.43 0 0
CUI: C0543541
Disease: HYPERGLYCINURIA (disorder)
HYPERGLYCINURIA (disorder) 		14 0 5 0.33 0 0
CUI: C0268528
Disease: Hyperprolinemia
Hyperprolinemia 		4 0 2 0.25 0 0
CUI: C0523852
Disease: Proline measurement
Proline measurement 		1 0 1 0.17 0 0
CUI: C1833247
Disease: SCHIZOPHRENIA 4 (disorder)
SCHIZOPHRENIA 4 (disorder) 		1 0 1 0.17 0 0
CUI: C1856194
Disease: Neutral hyperaminoaciduria
Neutral hyperaminoaciduria 		1 0 1 0.17 0 0
CUI: C3148959
Disease: IMINOGLYCINURIA, DIGENIC
IMINOGLYCINURIA, DIGENIC 		1 0 1 0.17 0 0
CUI: C0268525
Disease: 5-oxoprolinase deficiency
5-oxoprolinase deficiency 		2 0 1 0.14 0 0
CUI: C0268529
Disease: Proline dehydrogenase deficiency
Proline dehydrogenase deficiency 		2 0 1 0.14 0 0
CUI: C0398746
Disease: Gluthathione synthetase deficiency
Gluthathione synthetase deficiency 		2 0 1 0.14 0 0
CUI: C0428209
Disease: Leucine measurement
Leucine measurement 		2 0 1 0.14 0 0
CUI: C4703642
Disease: Increased level of L-pyroglutamic acid in urine
Increased level of L-pyroglutamic acid in urine 		2 0 1 0.14 0 0
CUI: C0523459
Disease: Alanine measurement
Alanine measurement 		3 0 1 0.12 0 0
CUI: C2931835
Disease: Hyperprolinemia type 2
Hyperprolinemia type 2 		3 0 1 0.12 0 0
CUI: C1833683
Disease: NEPHROLITHIASIS, CALCIUM OXALATE
NEPHROLITHIASIS, CALCIUM OXALATE 		33 0 4 0.11 0 0
CUI: C0085407
Disease: Microsporidiosis
Microsporidiosis 		4 0 1 0.11 0 0
CUI: C0202174
Disease: blood phenylalanine measurement by Guthrie microbiologic assay
blood phenylalanine measurement by Guthrie microbiologic assay 		4 0 1 0.11 0 0
CUI: C0337446
Disease: Tyrosine measurement
Tyrosine measurement 		4 0 1 0.11 0 0
CUI: C0398626
Disease: Heparin cofactor II deficiency (disorder)
Heparin cofactor II deficiency (disorder) 		4 0 1 0.11 0 0
CUI: C0523920
Disease: Threonine measurement
Threonine measurement 		4 0 1 0.11 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 2 8.3E-02 0 0
CUI: C0017675
Disease: Glossitis
Glossitis 		7 0 1 8.3E-02 0 0
CUI: C0522153
Disease: Urine Discoloration
Urine Discoloration 		10 0 1 6.7E-02 0 0
CUI: C0543918
Disease: SCHIZOPHRENIA 10
SCHIZOPHRENIA 10 		10 0 1 6.7E-02 0 0