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: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0 150 0 0 1 4.1E-03
CUI: C0523573
Disease: Citrulline measurement
Citrulline measurement 		0 1 0 0 1 1.1E-02
CUI: C0006542
Disease: Byssinosis
Byssinosis 		1 0 1 1.9E-02 0 0
CUI: C0030328
Disease: Panniculitis, Nodular Nonsuppurative
Panniculitis, Nodular Nonsuppurative 		1 0 1 1.9E-02 0 0
CUI: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		1 2 1 1.9E-02 1 1.1E-02
CUI: C0241876
Disease: Obstructive emphysema
Obstructive emphysema 		1 0 1 1.9E-02 0 0
CUI: C0268461
Disease: Disorder of phenylalanine metabolism
Disorder of phenylalanine metabolism 		1 0 1 1.9E-02 0 0
CUI: C0343972
Disease: Schistosomal splenomegaly
Schistosomal splenomegaly 		1 0 1 1.9E-02 0 0
CUI: C0392609
Disease: Acquired hypofibrinogenemia
Acquired hypofibrinogenemia 		1 0 1 1.9E-02 0 0
CUI: C0409896
Disease: Familial chondrocalcinosis
Familial chondrocalcinosis 		1 0 1 1.9E-02 0 0
CUI: C0523801
Disease: Ornithine measurement
Ornithine measurement 		1 2 1 1.9E-02 2 2.2E-02
CUI: C0523852
Disease: Proline measurement
Proline measurement 		1 3 1 1.9E-02 3 3.3E-02
CUI: C0580190
Disease: 3-Phosphoglycerate dehydrogenase deficiency
3-Phosphoglycerate dehydrogenase deficiency 		1 0 1 1.9E-02 0 0
CUI: C0743188
Disease: diarrhea persistent
diarrhea persistent 		1 0 1 1.9E-02 0 0
CUI: C0744314
Disease: Gastroenterocolitis
Gastroenterocolitis 		1 0 1 1.9E-02 0 0
CUI: C1291463
Disease: Deficiency of phosphoserine phosphatase
Deficiency of phosphoserine phosphatase 		1 0 1 1.9E-02 0 0
CUI: C1833236
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 6 (disorder) 		1 0 1 1.9E-02 0 0
CUI: C1833247
Disease: SCHIZOPHRENIA 4 (disorder)
SCHIZOPHRENIA 4 (disorder) 		1 0 1 1.9E-02 0 0
CUI: C1849813
Disease: Glycogen Storage Disease of Heart, Lethal Congenital
Glycogen Storage Disease of Heart, Lethal Congenital 		1 0 1 1.9E-02 0 0
CUI: C1849926
Disease: Phenylpyruvic acidemia
Phenylpyruvic acidemia 		1 0 1 1.9E-02 0 0
CUI: C1850533
Disease: Yellow subcutaneous tissue covered by thin, scaly skin
Yellow subcutaneous tissue covered by thin, scaly skin 		1 0 1 1.9E-02 0 0
CUI: C2678416
Disease: Hyperphenylalaninemia, Non-Pku Mild
Hyperphenylalaninemia, Non-Pku Mild 		1 0 1 1.9E-02 0 0
CUI: C2936458
Disease: Fasciculoventricular Accessory Pathway
Fasciculoventricular Accessory Pathway 		1 0 1 1.9E-02 0 0
CUI: C2936459
Disease: Nodoventricular Accessory Pathway
Nodoventricular Accessory Pathway 		1 0 1 1.9E-02 0 0
CUI: C3150714
Disease: FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5
FASTING PLASMA GLUCOSE LEVEL QUANTITATIVE TRAIT LOCUS 5 		1 2 1 1.9E-02 1 1.1E-02