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: C0337443
Disease: Sodium measurement
Sodium measurement 		53 0 11 0.21 0 0
CUI: C0268016
Disease: Chronic hypokalemia
Chronic hypokalemia 		1 0 1 9.1E-02 0 0
CUI: C0268309
Disease: Inherited disorder of bilirubin metabolism
Inherited disorder of bilirubin metabolism 		1 0 1 9.1E-02 0 0
CUI: C0338329
Disease: recurrent childhood brain stem glioma
recurrent childhood brain stem glioma 		1 0 1 9.1E-02 0 0
CUI: C0473118
Disease: Physiological hyperbilirubinemia (disorder)
Physiological hyperbilirubinemia (disorder) 		1 0 1 9.1E-02 0 0
CUI: C1282908
Disease: De Vaal's syndrome
De Vaal's syndrome 		1 0 1 9.1E-02 0 0
CUI: C1531394
Disease: Perinatal jaundice
Perinatal jaundice 		1 0 1 9.1E-02 0 0
CUI: C1836006
Disease: NANOPHTHALMOS 2 (disorder)
NANOPHTHALMOS 2 (disorder) 		1 0 1 9.1E-02 0 0
CUI: C1839252
Disease: Hump-shaped mound of bone in central and posterior portions of vertebral endplate
Hump-shaped mound of bone in central and posterior portions of vertebral endplate 		1 0 1 9.1E-02 0 0
CUI: C1867904
Disease: LONG QT SYNDROME 5
LONG QT SYNDROME 5 		1 0 1 9.1E-02 0 0
CUI: C1970005
Disease: Asphyxiating Thoracic Dystrophy 2
Asphyxiating Thoracic Dystrophy 2 		1 0 1 9.1E-02 0 0
CUI: C1970236
Disease: Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen
Microphthalmia, Posterior, With Retinitis Pigmentosa, Foveoschisis, And Optic Disc Drusen 		1 0 1 9.1E-02 0 0
CUI: C2674407
Disease: Foveoschisis
Foveoschisis 		1 0 1 9.1E-02 0 0
CUI: C2676723
Disease: JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder)
JERVELL AND LANGE-NIELSEN SYNDROME 2 (disorder) 		1 0 1 9.1E-02 0 0
CUI: C3150956
Disease: LONG QT SYNDROME 5, ACQUIRED, SUSCEPTIBILITY TO
LONG QT SYNDROME 5, ACQUIRED, SUSCEPTIBILITY TO 		1 0 1 9.1E-02 0 0
CUI: C3502107
Disease: Breastfeeding Jaundice
Breastfeeding Jaundice 		1 0 1 9.1E-02 0 0
CUI: C3888554
Disease: UGT1A1 gene polymorphism
UGT1A1 gene polymorphism 		1 0 1 9.1E-02 0 0
CUI: C4014954
Disease: NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE
NEUTROPENIA, SEVERE CONGENITAL, 6, AUTOSOMAL RECESSIVE 		1 0 1 9.1E-02 0 0
CUI: C4225308
Disease: NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE VIII 		1 0 1 9.1E-02 0 0
CUI: C4225310
Disease: MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 15, PRIMARY, AUTOSOMAL RECESSIVE 		1 0 1 9.1E-02 0 0
CUI: C4225311
Disease: CILIARY DYSKINESIA, PRIMARY, 32
CILIARY DYSKINESIA, PRIMARY, 32 		1 0 1 9.1E-02 0 0
CUI: C0231243
Disease: Early complication
Early complication 		2 0 1 8.3E-02 0 0
CUI: C0270202
Disease: Hemolytic disease of fetus OR newborn due to ABO immunization
Hemolytic disease of fetus OR newborn due to ABO immunization 		2 0 1 8.3E-02 0 0
CUI: C0272167
Disease: Reticular dysgenesis
Reticular dysgenesis 		2 0 1 8.3E-02 0 0
CUI: C0559506
Disease: Neonatal unconjugated hyperbilirubinemia
Neonatal unconjugated hyperbilirubinemia 		2 0 1 8.3E-02 0 0