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: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		0 4 0 0 1 4.2E-02
CUI: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 4.8E-02
CUI: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		0 1 0 0 1 4.8E-02
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia 		0 1 0 0 1 4.8E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 4.8E-02
CUI: C0268186
Disease: Congenital glucose-galactose malabsorption
Congenital glucose-galactose malabsorption 		0 12 0 0 1 3.1E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 9.5E-02
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome 		0 2 0 0 2 9.5E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 9.5E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 4.5E-02
CUI: C1401162
Disease: Carbohydrate intolerance
Carbohydrate intolerance 		0 1 0 0 1 4.8E-02
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		401 4389 1 1.9E-03 2 4.5E-04
CUI: C0037369
Disease: Smoking
Smoking 		391 0 1 2.0E-03 0 0
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure 		391 0 1 2.0E-03 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders 		362 0 1 2.1E-03 0 0
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 1 2.5E-03 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot 		285 0 1 2.5E-03 0 0
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		265 457 1 2.6E-03 1 2.1E-03
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		261 0 1 2.6E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 2.7E-03 0 0
CUI: C0489786
Disease: Height
Height 		249 0 1 2.7E-03 0 0
CUI: C0025990
Disease: Micrognathism
Micrognathism 		586 0 2 2.8E-03 0 0
CUI: C0454644
Disease: Delayed speech and language development
Delayed speech and language development 		560 0 2 3.0E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 3.0E-03 0 0
CUI: C0239676
Disease: High forehead
High forehead 		211 0 1 3.0E-03 0 0