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: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain 		4 0 1 0.14 0 0
CUI: C0302274
Disease: Glutamine measurement
Glutamine measurement 		5 5 1 0.12 1 9.1E-02
CUI: C0549397
Disease: Deviated nasal septum
Deviated nasal septum 		5 0 1 0.12 0 0
CUI: C0878676
Disease: 6-pyruvoyl-tetrahydropterin synthase deficiency
6-pyruvoyl-tetrahydropterin synthase deficiency 		5 0 1 0.12 0 0
CUI: C3697119
Disease: Pulmonary arterial hypertension associated with congenital heart disease
Pulmonary arterial hypertension associated with congenital heart disease 		5 0 1 0.12 0 0
CUI: C0085547
Disease: Phenylketonuria, Maternal
Phenylketonuria, Maternal 		6 0 1 0.11 0 0
CUI: C0268464
Disease: Transient hyperphenylalaninemia
Transient hyperphenylalaninemia 		6 0 1 0.11 0 0
CUI: C0268465
Disease: Phenylketonuria II
Phenylketonuria II 		6 0 1 0.11 0 0
CUI: C0268534
Disease: Prolinuria
Prolinuria 		6 0 1 0.11 0 0
CUI: C1862324
Disease: Elliptocytosis 4
Elliptocytosis 4 		6 0 1 0.11 0 0
CUI: C4706503
Disease: Distal monosomy 3p syndrome
Distal monosomy 3p syndrome 		6 0 1 0.11 0 0
CUI: C0268242
Disease: Niemann-Pick Disease, Type A
Niemann-Pick Disease, Type A 		7 0 1 1.0E-01 0 0
CUI: C4703632
Disease: Increased level of hippuric acid in urine
Increased level of hippuric acid in urine 		7 0 1 1.0E-01 0 0
CUI: C0002514
Disease: Amino Acid Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors 		20 0 2 9.1E-02 0 0
CUI: C0333161
Disease: Pseudocyst
Pseudocyst 		8 0 1 9.1E-02 0 0
CUI: C0948585
Disease: Hydroxyprolinuria
Hydroxyprolinuria 		8 0 1 9.1E-02 0 0
CUI: C3887658
Disease: PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT
PULMONARY VENOOCCLUSIVE DISEASE 1, AUTOSOMAL DOMINANT 		8 0 1 9.1E-02 0 0
CUI: C4289946
Disease: B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative
B Acute Lymphoblastic Leukemia, Philadelphia Chromosome Negative 		8 0 1 9.1E-02 0 0
CUI: C0523888
Disease: Serine measurement
Serine measurement 		9 18 1 8.3E-02 1 4.2E-02
CUI: C0751436
Disease: Hyperphenylalaninemia, Non-Phenylketonuric
Hyperphenylalaninemia, Non-Phenylketonuric 		9 0 1 8.3E-02 0 0
CUI: C4551693
Disease: Wolfram Syndrome 1
Wolfram Syndrome 1 		9 0 1 8.3E-02 0 0
CUI: C0543918
Disease: SCHIZOPHRENIA 10
SCHIZOPHRENIA 10 		10 0 1 7.7E-02 0 0
CUI: C0027854
Disease: Neurologic Manifestations
Neurologic Manifestations 		12 0 1 6.7E-02 0 0
CUI: C0701818
Disease: Choledocholithiasis
Choledocholithiasis 		12 0 1 6.7E-02 0 0
CUI: C1701939
Disease: Familial pulmonary arterial hypertension
Familial pulmonary arterial hypertension 		12 0 1 6.7E-02 0 0