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: C0523852
Disease: Proline measurement
Proline measurement 		1 0 1 0.50 0 0
CUI: C1833247
Disease: SCHIZOPHRENIA 4 (disorder)
SCHIZOPHRENIA 4 (disorder) 		1 7 1 0.50 6 0.50
CUI: C0428209
Disease: Leucine measurement
Leucine measurement 		2 0 1 0.33 0 0
CUI: C0523459
Disease: Alanine measurement
Alanine measurement 		3 0 1 0.25 0 0
CUI: C0202174
Disease: blood phenylalanine measurement by Guthrie microbiologic assay
blood phenylalanine measurement by Guthrie microbiologic assay 		4 0 1 0.20 0 0
CUI: C0268528
Disease: Hyperprolinemia
Hyperprolinemia 		4 3 1 0.20 2 0.17
CUI: C0337446
Disease: Tyrosine measurement
Tyrosine measurement 		4 0 1 0.20 0 0
CUI: C0398626
Disease: Heparin cofactor II deficiency (disorder)
Heparin cofactor II deficiency (disorder) 		4 0 1 0.20 0 0
CUI: C0523920
Disease: Threonine measurement
Threonine measurement 		4 0 1 0.20 0 0
CUI: C4021592
Disease: Unilateral primary pulmonary dysgenesis
Unilateral primary pulmonary dysgenesis 		5 0 1 0.17 0 0
CUI: C0268534
Disease: Prolinuria
Prolinuria 		6 0 1 0.14 0 0
CUI: C4025695
Disease: Right aortic arch with mirror image branching
Right aortic arch with mirror image branching 		7 0 1 0.12 0 0
CUI: C0948585
Disease: Hydroxyprolinuria
Hydroxyprolinuria 		8 0 1 0.11 0 0
CUI: C0543918
Disease: SCHIZOPHRENIA 10
SCHIZOPHRENIA 10 		10 0 1 9.1E-02 0 0
CUI: C0027854
Disease: Neurologic Manifestations
Neurologic Manifestations 		12 0 1 7.7E-02 0 0
CUI: C0750905
Disease: Amino Acid Metabolism, Inherited Disorders
Amino Acid Metabolism, Inherited Disorders 		13 0 1 7.1E-02 0 0
CUI: C0007398
Disease: Catatonia
Catatonia 		14 0 1 6.7E-02 0 0
CUI: C0543541
Disease: HYPERGLYCINURIA (disorder)
HYPERGLYCINURIA (disorder) 		14 0 1 6.7E-02 0 0
CUI: C0795907
Disease: CONOTRUNCAL ANOMALY FACE SYNDROME
CONOTRUNCAL ANOMALY FACE SYNDROME 		18 0 1 5.3E-02 0 0
CUI: C0020617
Disease: Hypoglycemic coma
Hypoglycemic coma 		19 0 1 5.0E-02 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 1 4.8E-02 0 0
CUI: C1860475
Disease: Retinal vascular tortuosity
Retinal vascular tortuosity 		20 0 1 4.8E-02 0 0
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		46 0 2 4.3E-02 0 0
CUI: C0042454
Disease: Velopharyngeal Insufficiency
Velopharyngeal Insufficiency 		27 0 1 3.6E-02 0 0
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		61 0 2 3.3E-02 0 0