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: C0151772
Disease: Manic psychosis
Manic psychosis 		1 0 1 2.2E-02 0 0
CUI: C0343431
Disease: Disseminated mycobacteriosis
Disseminated mycobacteriosis 		1 0 1 2.2E-02 0 0
CUI: C1096262
Disease: Escherichia bacteraemia
Escherichia bacteraemia 		1 0 1 2.2E-02 0 0
CUI: C1970483
Disease: Vesicoureteral Reflux 2
Vesicoureteral Reflux 2 		1 0 1 2.2E-02 0 0
CUI: C3807327
Disease: ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1
ADVANCED SLEEP PHASE SYNDROME, FAMILIAL, 1 		1 0 1 2.2E-02 0 0
CUI: C3809928
Disease: AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III
AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME, TYPE III 		1 0 1 2.2E-02 0 0
CUI: C4706527
Disease: Startle epilepsy
Startle epilepsy 		1 0 1 2.2E-02 0 0
CUI: C0041848
Disease: Unspecified idiopathic peripheral neuropathy
Unspecified idiopathic peripheral neuropathy 		2 0 1 2.2E-02 0 0
CUI: C0235329
Disease: Small bowel obstruction
Small bowel obstruction 		2 0 1 2.2E-02 0 0
CUI: C0751226
Disease: Hypersomnia, Recurrent
Hypersomnia, Recurrent 		2 0 1 2.2E-02 0 0
CUI: C0859974
Disease: Neonatal intestinal obstruction
Neonatal intestinal obstruction 		2 0 1 2.2E-02 0 0
CUI: C1845165
Disease: PARKINSON DISEASE 12
PARKINSON DISEASE 12 		2 0 1 2.2E-02 0 0
CUI: C1853507
Disease: Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations
Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations 		2 0 2 4.4E-02 0 0
CUI: C3150618
Disease: Maturity-onset diabetes of the young, type 11
Maturity-onset diabetes of the young, type 11 		2 0 1 2.2E-02 0 0
CUI: C3495887
Disease: ARIA-H
ARIA-H 		2 0 1 2.2E-02 0 0
CUI: C3873497
Disease: Severe acute respiratory infection
Severe acute respiratory infection 		2 0 1 2.2E-02 0 0
CUI: C4280575
Disease: Progressive brain disease
Progressive brain disease 		2 0 1 2.2E-02 0 0
CUI: C4749023
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70 		2 0 1 2.2E-02 0 0
CUI: C0795887
Disease: Complex Glycerol Kinase Deficiency
Complex Glycerol Kinase Deficiency 		3 0 1 2.1E-02 0 0
CUI: C0796241
Disease: MENTAL RETARDATION, X-LINKED 34 (disorder)
MENTAL RETARDATION, X-LINKED 34 (disorder) 		3 0 1 2.1E-02 0 0
CUI: C1838571
Disease: Ceroid Lipofuscinosis, Neuronal, 7
Ceroid Lipofuscinosis, Neuronal, 7 		3 0 1 2.1E-02 0 0
CUI: C1850447
Disease: Rectilinear intracellular accumulation of autofluorescent lipopigment storage material
Rectilinear intracellular accumulation of autofluorescent lipopigment storage material 		3 0 1 2.1E-02 0 0
CUI: C2203937
Disease: Night Eating Syndrome
Night Eating Syndrome 		3 0 1 2.1E-02 0 0
CUI: C2750088
Disease: HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO
HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO 		3 0 1 2.1E-02 0 0
CUI: C4021781
Disease: Abnormal nervous system electrophysiology
Abnormal nervous system electrophysiology 		3 0 1 2.1E-02 0 0