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: C0026552
Disease: Morphine Dependence
Morphine Dependence 		44 0 7 0.16 0 0
CUI: C0348165
Disease: Central Nervous System Viral Diseases
Central Nervous System Viral Diseases 		7 0 2 0.15 0 0
CUI: C0018121
Disease: Gradenigo Syndrome
Gradenigo Syndrome 		1 0 1 0.12 0 0
CUI: C0026686
Disease: Mucocele of salivary gland
Mucocele of salivary gland 		1 0 1 0.12 0 0
CUI: C0149704
Disease: Gingivostomatitis
Gingivostomatitis 		1 0 1 0.12 0 0
CUI: C0155804
Disease: Acute maxillary sinusitis
Acute maxillary sinusitis 		1 0 1 0.12 0 0
CUI: C0234516
Disease: Speech dysfunction
Speech dysfunction 		1 0 1 0.12 0 0
CUI: C0241518
Disease: Retraction of tympanic membrane
Retraction of tympanic membrane 		1 0 1 0.12 0 0
CUI: C0264622
Disease: Psychogenic voice disorder
Psychogenic voice disorder 		1 0 1 0.12 0 0
CUI: C0342650
Disease: Periarticular calcification
Periarticular calcification 		1 0 1 0.12 0 0
CUI: C0342959
Disease: Sepsis-associated organ dysfunction
Sepsis-associated organ dysfunction 		1 0 1 0.12 0 0
CUI: C0423479
Disease: Ear symptom
Ear symptom 		1 0 1 0.12 0 0
CUI: C1837893
Disease: SCHIZOPHRENIA 12
SCHIZOPHRENIA 12 		1 0 1 0.12 0 0
CUI: C1959587
Disease: Ventricular Free Wall Rupture
Ventricular Free Wall Rupture 		1 0 1 0.12 0 0
CUI: C2242813
Disease: Ranula (disorder)
Ranula (disorder) 		1 0 1 0.12 0 0
CUI: C2751322
Disease: Metaphyseal Anadysplasia 2
Metaphyseal Anadysplasia 2 		1 0 1 0.12 0 0
CUI: C3532225
Disease: Valvular cardiomyopathy
Valvular cardiomyopathy 		1 0 1 0.12 0 0
CUI: C3714630
Disease: Respirovirus Infections
Respirovirus Infections 		1 0 1 0.12 0 0
CUI: C4024937
Disease: Chronic hepatic encephalopathy
Chronic hepatic encephalopathy 		1 0 1 0.12 0 0
CUI: C4551494
Disease: Desquamative gingivitis
Desquamative gingivitis 		1 0 1 0.12 0 0
CUI: C4704679
Disease: Opium Use
Opium Use 		1 0 1 0.12 0 0
CUI: C4749281
Disease: Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation
Early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation 		1 0 1 0.12 0 0
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		2 0 1 0.11 0 0
CUI: C0017577
Disease: Chronic desquamative gingivitis
Chronic desquamative gingivitis 		2 0 1 0.11 0 0
CUI: C0027438
Disease: Nasopharyngeal Diseases
Nasopharyngeal Diseases 		2 0 1 0.11 0 0