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: C0454600
Disease: Extrapyramidal dysarthria
Extrapyramidal dysarthria 		2 0 2 0.20 0 0
CUI: C0586392
Disease: Parkinsonian tremor
Parkinsonian tremor 		2 0 2 0.20 0 0
CUI: C1857277
Disease: Donnai-Barrow syndrome
Donnai-Barrow syndrome 		2 0 2 0.20 0 0
CUI: C3536587
Disease: Grand mal status epilepticus, refractory
Grand mal status epilepticus, refractory 		2 0 2 0.20 0 0
CUI: C1536088
Disease: Positive myoclonus
Positive myoclonus 		3 0 2 0.18 0 0
CUI: C4049471
Disease: End stage Parkinson's disease
End stage Parkinson's disease 		3 0 2 0.18 0 0
CUI: C0920233
Disease: Pisa syndrome
Pisa syndrome 		4 0 2 0.17 0 0
CUI: C1842534
Disease: DYSTONIA 18 (disorder)
DYSTONIA 18 (disorder) 		6 19 2 0.14 2 8.3E-02
CUI: C0013369
Disease: Dysentery
Dysentery 		7 0 2 0.13 0 0
CUI: C0264162
Disease: Camptocormia
Camptocormia 		8 0 2 0.12 0 0
CUI: C4020778
Disease: maternal hyperglycemia
maternal hyperglycemia 		8 0 2 0.12 0 0
CUI: C0221169
Disease: Hemiballismus
Hemiballismus 		9 0 2 0.12 0 0
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