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: C0005911
Disease: Body Weight Changes
Body Weight Changes 		1 0 1 1.0E-01 0 0
CUI: C0238110
Disease: Chronic epididymitis
Chronic epididymitis 		1 0 1 1.0E-01 0 0
CUI: C0267896
Disease: Mucocele of gallbladder
Mucocele of gallbladder 		1 0 1 1.0E-01 0 0
CUI: C0268179
Disease: Lactase Deficiency, Congenital
Lactase Deficiency, Congenital 		1 0 1 1.0E-01 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 1.0E-01 0 0
CUI: C0679254
Disease: Disease recurrence
Disease recurrence 		1 0 1 1.0E-01 0 0
CUI: C0948393
Disease: Oedematous pancreatitis
Oedematous pancreatitis 		1 0 1 1.0E-01 0 0
CUI: C1735903
Disease: Chronic acidosis
Chronic acidosis 		1 0 1 1.0E-01 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 7 1 1.0E-01 2 0.17
CUI: C1837206
Disease: Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly
Cryohydrocytosis, Stomatin-Deficient, with Mental Retardation, Seizures, Cataracts, and Massive Hepatosplenomegaly 		1 8 1 1.0E-01 2 0.15
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 1.0E-01 0 0
CUI: C3149117
Disease: GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE
GLUT1 DEFICIENCY SYNDROME 1, AUTOSOMAL RECESSIVE 		1 19 1 1.0E-01 2 8.3E-02
CUI: C3249879
Disease: Combat Fatigue
Combat Fatigue 		1 0 1 1.0E-01 0 0
CUI: C3266628
Disease: Persistent asthma
Persistent asthma 		1 0 1 1.0E-01 0 0
CUI: C3553859
Disease: EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12
EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 12 		1 11 1 1.0E-01 1 5.9E-02
CUI: C4015357
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 31
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31 		1 0 1 1.0E-01 0 0
CUI: C4016279
Disease: LEPTIN DYSFUNCTION
LEPTIN DYSFUNCTION 		1 0 1 1.0E-01 0 0
CUI: C4025176
Disease: Non-acidotic proximal tubulopathy
Non-acidotic proximal tubulopathy 		1 0 1 1.0E-01 0 0
CUI: C4302261
Disease: Primary lactase deficiency
Primary lactase deficiency 		1 0 1 1.0E-01 0 0
CUI: C4551966
Disease: GLUT1 DEFICIENCY SYNDROME 1
GLUT1 DEFICIENCY SYNDROME 1 		1 35 1 1.0E-01 5 0.14
CUI: C4708498
Disease: PURA syndrome
PURA syndrome 		1 0 1 1.0E-01 0 0
CUI: C0266752
Disease: Twin placenta
Twin placenta 		2 0 1 9.1E-02 0 0
CUI: C0391870
Disease: Abnormality of red blood cells
Abnormality of red blood cells 		2 0 1 9.1E-02 0 0
CUI: C0431649
Disease: Vaginal septum
Vaginal septum 		2 0 1 9.1E-02 0 0
CUI: C0454600
Disease: Extrapyramidal dysarthria
Extrapyramidal dysarthria 		2 0 2 0.20 0 0