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: C0202115
Disease: Lactic acid measurement
Lactic acid measurement 		0 2 0 0 1 1.4E-02
CUI: C0523573
Disease: Citrulline measurement
Citrulline measurement 		0 1 0 0 1 1.5E-02
CUI: C0523920
Disease: Threonine measurement
Threonine measurement 		0 5 0 0 1 1.4E-02
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		0 32 0 0 1 1.0E-02
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		0 46 0 0 1 8.8E-03
CUI: C0039614
Disease: Tetanus
Tetanus 		1 0 1 3.1E-02 0 0
CUI: C0406821
Disease: Rhabdomyomatous mesenchymal hamartoma
Rhabdomyomatous mesenchymal hamartoma 		1 0 1 3.1E-02 0 0
CUI: C0580190
Disease: 3-Phosphoglycerate dehydrogenase deficiency
3-Phosphoglycerate dehydrogenase deficiency 		1 0 1 3.1E-02 0 0
CUI: C0744314
Disease: Gastroenterocolitis
Gastroenterocolitis 		1 0 1 3.1E-02 0 0
CUI: C1262106
Disease: Neuromuscular toxicity
Neuromuscular toxicity 		1 0 1 3.1E-02 0 0
CUI: C1274890
Disease: Midline cervical cleft
Midline cervical cleft 		1 0 1 3.1E-02 0 0
CUI: C1291463
Disease: Deficiency of phosphoserine phosphatase
Deficiency of phosphoserine phosphatase 		1 0 1 3.1E-02 0 0
CUI: C1456270
Disease: Fatty acid oxidation disorder
Fatty acid oxidation disorder 		1 0 1 3.1E-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 3.1E-02 0 0
CUI: C1860081
Disease: Medium chain dicarboxylic aciduria
Medium chain dicarboxylic aciduria 		1 0 1 3.1E-02 0 0
CUI: C2959380
Disease: Folliculosebaceous cystic hamartoma
Folliculosebaceous cystic hamartoma 		1 0 1 3.1E-02 0 0
CUI: C3541908
Disease: Sperm Motility Measurement
Sperm Motility Measurement 		1 0 1 3.1E-02 0 0
CUI: C3552528
Disease: Generalized ichthyosis
Generalized ichthyosis 		1 0 1 3.1E-02 0 0
CUI: C3714958
Disease: PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO
PULMONARY HYPERTENSION, NEONATAL, SUSCEPTIBILITY TO 		1 0 1 3.1E-02 0 0
CUI: C3715155
Disease: AMYOTROPHIC LATERAL SCLEROSIS 19
AMYOTROPHIC LATERAL SCLEROSIS 19 		1 0 1 3.1E-02 0 0
CUI: C4016097
Disease: FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE
FIBRINOGEN MILANO XII, DIGENIC PHENOTYPE 		1 0 1 3.1E-02 0 0
CUI: C4022414
Disease: Elevated urinary 3-hydroxybutyric acid
Elevated urinary 3-hydroxybutyric acid 		1 0 1 3.1E-02 0 0
CUI: C4023465
Disease: EEG with occipital slowing
EEG with occipital slowing 		1 0 1 3.1E-02 0 0
CUI: C4280778
Disease: Modic type vertebral endplate changes
Modic type vertebral endplate changes 		1 0 1 3.1E-02 0 0
CUI: C4324411
Disease: Blood type incompatibility
Blood type incompatibility 		1 0 1 3.1E-02 0 0