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: C0022492
Disease: Kandinsky Syndrome
Kandinsky Syndrome 		1 0 1 2.8E-02 0 0
CUI: C0023213
Disease: Ventricular Outflow Obstruction, Left
Ventricular Outflow Obstruction, Left 		1 0 1 2.8E-02 0 0
CUI: C0028313
Disease: Organic Brain Syndrome, Nonpsychotic
Organic Brain Syndrome, Nonpsychotic 		1 0 1 2.8E-02 0 0
CUI: C0029230
Disease: Organic Mental Disorders, Psychotic
Organic Mental Disorders, Psychotic 		1 0 1 2.8E-02 0 0
CUI: C0033943
Disease: Psychoses, Traumatic
Psychoses, Traumatic 		1 0 1 2.8E-02 0 0
CUI: C0035619
Disease: Ventricular Outflow Obstruction, Right
Ventricular Outflow Obstruction, Right 		1 0 1 2.8E-02 0 0
CUI: C0042512
Disease: Ventricular Outflow Obstruction
Ventricular Outflow Obstruction 		1 0 1 2.8E-02 0 0
CUI: C0235242
Disease: Syncope, Effort
Syncope, Effort 		1 0 1 2.8E-02 0 0
CUI: C0264787
Disease: Nonobstructive cardiomyopathy
Nonobstructive cardiomyopathy 		1 0 1 2.8E-02 0 0
CUI: C0270221
Disease: Syndrome of infant of diabetic mother
Syndrome of infant of diabetic mother 		1 0 1 2.8E-02 0 0
CUI: C0270730
Disease: MPTP Poisoning
MPTP Poisoning 		1 0 1 2.8E-02 0 0
CUI: C0276876
Disease: Infection by Leishmania infantum
Infection by Leishmania infantum 		1 0 1 2.8E-02 0 0
CUI: C0391860
Disease: Diffuse inflammation
Diffuse inflammation 		1 0 1 2.8E-02 0 0
CUI: C0518959
Disease: Left atrial myxoma
Left atrial myxoma 		1 0 1 2.8E-02 0 0
CUI: C0555197
Disease: Florid cemento-osseous dysplasia
Florid cemento-osseous dysplasia 		1 0 1 2.8E-02 0 0
CUI: C0751864
Disease: MPTP-Induced Degeneration of the Striatum
MPTP-Induced Degeneration of the Striatum 		1 0 1 2.8E-02 0 0
CUI: C0856123
Disease: Myotonia aggravated
Myotonia aggravated 		1 0 1 2.8E-02 0 0
CUI: C1386553
Disease: Caffeine dependence
Caffeine dependence 		1 0 1 2.8E-02 0 0
CUI: C1456270
Disease: Fatty acid oxidation disorder
Fatty acid oxidation disorder 		1 0 1 2.8E-02 0 0
CUI: C1827284
Disease: Refractory occipital lobe epilepsy
Refractory occipital lobe epilepsy 		1 0 1 2.8E-02 0 0
CUI: C1832733
Disease: Rhabdomyolysis, Cerivastatin-Induced
Rhabdomyolysis, Cerivastatin-Induced 		1 0 1 2.8E-02 0 0
CUI: C1833202
Disease: LCHAD DEFICIENCY WITH MATERNAL ACUTE FATTY LIVER OF PREGNANCY
LCHAD DEFICIENCY WITH MATERNAL ACUTE FATTY LIVER OF PREGNANCY 		1 0 1 2.8E-02 0 0
CUI: C1833508
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LATE-ONSET 		1 36 1 2.8E-02 1 2.0E-02
CUI: C1833511
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE 		1 54 1 2.8E-02 1 1.5E-02
CUI: C1833518
Disease: CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL 		1 24 1 2.8E-02 1 2.6E-02