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: C1969810
Disease: FEBRILE CONVULSIONS, FAMILIAL, 8
FEBRILE CONVULSIONS, FAMILIAL, 8 		0 13 0 0 1 4.0E-02
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 3.0E-02 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 3.0E-02 0 0
CUI: C0232308
Disease: P pulmonale by EKG (finding)
P pulmonale by EKG (finding) 		1 0 1 3.0E-02 0 0
CUI: C0233480
Disease: Hyperirritability
Hyperirritability 		1 0 1 3.0E-02 0 0
CUI: C0264402
Disease: Gas bubble disease
Gas bubble disease 		1 0 1 3.0E-02 0 0
CUI: C0265241
Disease: Franceschetti-Klein syndrome
Franceschetti-Klein syndrome 		1 0 1 3.0E-02 0 0
CUI: C0278193
Disease: Reflex Epilepsy, Reading
Reflex Epilepsy, Reading 		1 0 1 3.0E-02 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 3.0E-02 0 0
CUI: C0393697
Disease: Epilepsy with grand mal seizures on awakening (disorder)
Epilepsy with grand mal seizures on awakening (disorder) 		1 0 1 3.0E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 3.0E-02 0 0
CUI: C0748427
Disease: Right atrial enlargement
Right atrial enlargement 		1 0 1 3.0E-02 0 0
CUI: C0751863
Disease: Lead Poisoning, Nervous System, Adult
Lead Poisoning, Nervous System, Adult 		1 0 1 3.0E-02 0 0
CUI: C0855389
Disease: Renin decreased
Renin decreased 		1 0 1 3.0E-02 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 3.0E-02 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 3.0E-02 0 0
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 0 1 3.0E-02 0 0
CUI: C1843244
Disease: EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2 		1 10 1 3.0E-02 1 4.5E-02
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 3.0E-02 0 0
CUI: C1853701
Disease: Muscle hyperirritability
Muscle hyperirritability 		1 0 1 3.0E-02 0 0
CUI: C1858674
Disease: GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3
GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 3 		1 4 1 3.0E-02 1 6.2E-02
CUI: C1862491
Disease: Internally rotated shoulders
Internally rotated shoulders 		1 0 1 3.0E-02 0 0
CUI: C1866984
Disease: Sclerocornea, Autosomal Dominant
Sclerocornea, Autosomal Dominant 		1 0 1 3.0E-02 0 0
CUI: C1970160
Disease: Epilepsy, Childhood Absence, Susceptibility To, 4
Epilepsy, Childhood Absence, Susceptibility To, 4 		1 0 1 3.0E-02 0 0
CUI: C2676770
Disease: Birk-Barel Mental Retardation Dysmorphism Syndrome
Birk-Barel Mental Retardation Dysmorphism Syndrome 		1 0 1 3.0E-02 0 0