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: C0268534
Disease: Prolinuria
Prolinuria 		6 0 5 0.33 0 0
CUI: C0948585
Disease: Hydroxyprolinuria
Hydroxyprolinuria 		8 0 5 0.29 0 0
CUI: C0268654
Disease: Iminoglycinuria
Iminoglycinuria 		4 2 4 0.29 2 0.67
CUI: C0268559
Disease: Hyperglycinemia
Hyperglycinemia 		14 0 5 0.22 0 0
CUI: C0268561
Disease: Hyperglycinemia, Nonketotic, Type I
Hyperglycinemia, Nonketotic, Type I 		3 0 3 0.21 0 0
CUI: C0268562
Disease: Hyperglycinemia, Nonketotic, Type II
Hyperglycinemia, Nonketotic, Type II 		3 0 3 0.21 0 0
CUI: C0744897
Disease: Recurrent singultus
Recurrent singultus 		3 0 3 0.21 0 0
CUI: C0751747
Disease: Hyperglycinemia, Nonketotic, Type III
Hyperglycinemia, Nonketotic, Type III 		3 0 3 0.21 0 0
CUI: C0268560
Disease: Hyperglycinemia, Transient Neonatal
Hyperglycinemia, Transient Neonatal 		2 0 2 0.14 0 0
CUI: C2717876
Disease: Propionicaciduria
Propionicaciduria 		2 0 2 0.14 0 0
CUI: C0241775
Disease: Organic aciduria
Organic aciduria 		12 0 3 0.13 0 0
CUI: C0265428
Disease: Chromosome 9, partial trisomy 9p
Chromosome 9, partial trisomy 9p 		4 0 2 0.12 0 0
CUI: C0268528
Disease: Hyperprolinemia
Hyperprolinemia 		4 0 2 0.12 0 0
CUI: C0795830
Disease: CHROMOSOME 9p DELETION SYNDROME
CHROMOSOME 9p DELETION SYNDROME 		5 0 2 0.12 0 0
CUI: C0268579
Disease: Propionic acidemia
Propionic acidemia 		17 0 3 0.11 0 0
CUI: C3151140
Disease: PONTOCEREBELLAR HYPOPLASIA, TYPE 2D
PONTOCEREBELLAR HYPOPLASIA, TYPE 2D 		7 0 2 0.11 0 0
CUI: C4703632
Disease: Increased level of hippuric acid in urine
Increased level of hippuric acid in urine 		7 0 2 0.11 0 0
CUI: C0751748
Disease: Nonketotic Hyperglycinemia
Nonketotic Hyperglycinemia 		21 0 3 9.4E-02 0 0
CUI: C3887612
Disease: Psychomotor Agitation
Psychomotor Agitation 		26 0 3 8.1E-02 0 0
CUI: C0523852
Disease: Proline measurement
Proline measurement 		1 0 1 7.1E-02 0 0
CUI: C1456270
Disease: Fatty acid oxidation disorder
Fatty acid oxidation disorder 		1 0 1 7.1E-02 0 0
CUI: C1833247
Disease: SCHIZOPHRENIA 4 (disorder)
SCHIZOPHRENIA 4 (disorder) 		1 0 1 7.1E-02 0 0
CUI: C1856194
Disease: Neutral hyperaminoaciduria
Neutral hyperaminoaciduria 		1 0 1 7.1E-02 0 0
CUI: C1859499
Disease: 3-methylcrotonyl CoA carboxylase 2 deficiency
3-methylcrotonyl CoA carboxylase 2 deficiency 		1 0 1 7.1E-02 0 0
CUI: C1860081
Disease: Medium chain dicarboxylic aciduria
Medium chain dicarboxylic aciduria 		1 0 1 7.1E-02 0 0