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: C0523459
Disease: Alanine measurement
Alanine measurement 		3 3 2 0.40 2 0.25
CUI: C0337446
Disease: Tyrosine measurement
Tyrosine measurement 		4 11 2 0.33 3 0.20
CUI: C0523920
Disease: Threonine measurement
Threonine measurement 		4 5 2 0.33 2 0.20
CUI: C0268461
Disease: Disorder of phenylalanine metabolism
Disorder of phenylalanine metabolism 		1 0 1 0.25 0 0
CUI: C0392609
Disease: Acquired hypofibrinogenemia
Acquired hypofibrinogenemia 		1 0 1 0.25 0 0
CUI: C0523852
Disease: Proline measurement
Proline measurement 		1 3 1 0.25 1 0.11
CUI: C1833247
Disease: SCHIZOPHRENIA 4 (disorder)
SCHIZOPHRENIA 4 (disorder) 		1 0 1 0.25 0 0
CUI: C1849926
Disease: Phenylpyruvic acidemia
Phenylpyruvic acidemia 		1 0 1 0.25 0 0
CUI: C2678416
Disease: Hyperphenylalaninemia, Non-Pku Mild
Hyperphenylalaninemia, Non-Pku Mild 		1 0 1 0.25 0 0
CUI: C4022014
Disease: Maternal hyperphenylalaninemia
Maternal hyperphenylalaninemia 		1 0 1 0.25 0 0
CUI: C4025094
Disease: Reduced phenylalanine hydroxylase activity
Reduced phenylalanine hydroxylase activity 		1 0 1 0.25 0 0
CUI: C4025273
Disease: Atypical hyperphenylalaninemia
Atypical hyperphenylalaninemia 		1 0 1 0.25 0 0
CUI: C0268529
Disease: Proline dehydrogenase deficiency
Proline dehydrogenase deficiency 		2 0 1 0.20 0 0
CUI: C0428209
Disease: Leucine measurement
Leucine measurement 		2 3 1 0.20 1 0.11
CUI: C0523516
Disease: Asparagine measurement
Asparagine measurement 		2 4 1 0.20 1 1.0E-01
CUI: C0523697
Disease: Histidine measurement
Histidine measurement 		2 2 1 0.20 1 0.12
CUI: C3697982
Disease: Pulmonary arterial hypertension associated with connective tissue disease
Pulmonary arterial hypertension associated with connective tissue disease 		2 0 1 0.20 0 0
CUI: C0428210
Disease: Methionine measurement
Methionine measurement 		3 4 1 0.17 2 0.22
CUI: C0523760
Disease: Lysine measurement
Lysine measurement 		3 3 1 0.17 1 0.11
CUI: C0523957
Disease: Tryptophan measurement
Tryptophan measurement 		3 3 1 0.17 1 0.11
CUI: C1860162
Disease: Bifid distal phalanx of the thumb
Bifid distal phalanx of the thumb 		3 0 1 0.17 0 0
CUI: C0268528
Disease: Hyperprolinemia
Hyperprolinemia 		4 0 1 0.14 0 0
CUI: C0398626
Disease: Heparin cofactor II deficiency (disorder)
Heparin cofactor II deficiency (disorder) 		4 0 1 0.14 0 0
CUI: C1832394
Disease: Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 12 		4 0 1 0.14 0 0
CUI: C1842681
Disease: Hypoplastic helices
Hypoplastic helices 		4 0 1 0.14 0 0