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: C4749023
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70 		2 0 1 2.2E-02 0 0
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses 		51 0 2 2.1E-02 0 0
CUI: C0162672
Disease: MERRF Syndrome
MERRF Syndrome 		51 0 2 2.1E-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
CUI: C4522160
Disease: Invasive Mucinous Lung Adenocarcinoma
Invasive Mucinous Lung Adenocarcinoma 		3 0 1 2.1E-02 0 0
CUI: C4703587
Disease: Early chronotype
Early chronotype 		3 0 1 2.1E-02 0 0
CUI: C4721577
Disease: stage IV esophageal cancer
stage IV esophageal cancer 		3 0 1 2.1E-02 0 0
CUI: C0155883
Disease: Chronic obstructive asthma (with obstructive pulmonary disease)
Chronic obstructive asthma (with obstructive pulmonary disease) 		4 0 1 2.1E-02 0 0
CUI: C0270541
Disease: Rebound Insomnia
Rebound Insomnia 		4 0 1 2.1E-02 0 0
CUI: C0349255
Disease: Nonorganic Insomnia
Nonorganic Insomnia 		4 0 1 2.1E-02 0 0
CUI: C0393759
Disease: Transient Insomnia
Transient Insomnia 		4 0 1 2.1E-02 0 0
CUI: C0751251
Disease: Secondary Insomnia
Secondary Insomnia 		4 0 1 2.1E-02 0 0
CUI: C0751252
Disease: Sleep Initiation Dysfunction
Sleep Initiation Dysfunction 		4 0 1 2.1E-02 0 0
CUI: C0751774
Disease: Nocturnal Myoclonus Syndrome
Nocturnal Myoclonus Syndrome 		4 0 1 2.1E-02 0 0
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		4 0 1 2.1E-02 0 0
CUI: C2825910
Disease: Stem Cell Factor Measurement
Stem Cell Factor Measurement 		4 0 1 2.1E-02 0 0
CUI: C0005716
Disease: Blastomycosis
Blastomycosis 		5 0 1 2.0E-02 0 0
CUI: C0155922
Disease: Tooth development and eruption disorder
Tooth development and eruption disorder 		5 0 1 2.0E-02 0 0
CUI: C0268600
Disease: 3-methylcrotonyl CoA carboxylase 1 deficiency
3-methylcrotonyl CoA carboxylase 1 deficiency 		5 0 1 2.0E-02 0 0