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: C2751719
Disease: ALCOHOL DEPENDENCE, PROTECTION AGAINST
ALCOHOL DEPENDENCE, PROTECTION AGAINST 		3 0 3 1.00 0 0
CUI: C0751868
Disease: Alcohol Withdrawal-Induced Major Motor Seizure
Alcohol Withdrawal-Induced Major Motor Seizure 		1 0 1 0.33 0 0
CUI: C0751869
Disease: Status Epilepticus, Alcohol Withdrawal-Induced
Status Epilepticus, Alcohol Withdrawal-Induced 		1 0 1 0.33 0 0
CUI: C1332316
Disease: Apocrine breast carcinoma
Apocrine breast carcinoma 		1 0 1 0.33 0 0
CUI: C1410087
Disease: Spine stiffness
Spine stiffness 		1 0 1 0.33 0 0
CUI: C0031051
Disease: Pericementitis
Pericementitis 		3 0 1 0.20 0 0
CUI: C0268524
Disease: gamma-Glutamyltransferase deficiency
gamma-Glutamyltransferase deficiency 		3 0 1 0.20 0 0
CUI: C0202035
Disease: Gamma glutamyl transferase measurement
Gamma glutamyl transferase measurement 		5 0 1 0.14 0 0
CUI: C0235299
Disease: Right upper quadrant pain
Right upper quadrant pain 		6 0 1 0.12 0 0
CUI: C1867396
Disease: RADIAL-RENAL SYNDROME
RADIAL-RENAL SYNDROME 		6 0 1 0.12 0 0
CUI: C0017927
Disease: Glycogen Storage Disease Type VIII
Glycogen Storage Disease Type VIII 		7 0 1 0.11 0 0
CUI: C0428321
Disease: Measurement of liver enzyme
Measurement of liver enzyme 		7 0 1 0.11 0 0
CUI: C1287351
Disease: Finding of liver enzyme levels
Finding of liver enzyme levels 		7 0 1 0.11 0 0
CUI: C0586323
Disease: Alcohol Withdrawal Seizures
Alcohol Withdrawal Seizures 		8 0 1 1.0E-01 0 0
CUI: C4023620
Disease: Blood group antigen abnormality
Blood group antigen abnormality 		8 0 1 1.0E-01 0 0
CUI: C0020498
Disease: Hyperostosis, Diffuse Idiopathic Skeletal
Hyperostosis, Diffuse Idiopathic Skeletal 		9 0 1 9.1E-02 0 0
CUI: C0149841
Disease: Benign recurrent intrahepatic cholestasis
Benign recurrent intrahepatic cholestasis 		10 0 1 8.3E-02 0 0
CUI: C0264010
Disease: Hepatic osteodystrophy
Hepatic osteodystrophy 		10 0 1 8.3E-02 0 0
CUI: C1853942
Disease: CITRULLINEMIA, TYPE II, NEONATAL-ONSET
CITRULLINEMIA, TYPE II, NEONATAL-ONSET 		10 0 1 8.3E-02 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 7.7E-02 0 0
CUI: C0339273
Disease: Corneal dystrophy, Lattice type 3
Corneal dystrophy, Lattice type 3 		12 0 1 7.1E-02 0 0
CUI: C0393574
Disease: Huntington Disease, Late Onset
Huntington Disease, Late Onset 		12 0 1 7.1E-02 0 0
CUI: C0751207
Disease: Akinetic-Rigid Variant of Huntington Disease
Akinetic-Rigid Variant of Huntington Disease 		12 0 1 7.1E-02 0 0
CUI: C0751208
Disease: Juvenile Huntington Disease
Juvenile Huntington Disease 		12 0 1 7.1E-02 0 0
CUI: C4551984
Disease: Arthrogryposis with renal dysfunction and cholestasis syndrome
Arthrogryposis with renal dysfunction and cholestasis syndrome 		12 0 1 7.1E-02 0 0