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: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 7.1E-02 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 7.1E-02 0 0
CUI: C0233483
Disease: Free-floating anxiety
Free-floating anxiety 		1 0 1 7.1E-02 0 0
CUI: C0235204
Disease: Irrational thoughts
Irrational thoughts 		1 0 1 7.1E-02 0 0
CUI: C0238014
Disease: Acute cerebellar ataxia
Acute cerebellar ataxia 		1 0 1 7.1E-02 0 0
CUI: C0338999
Disease: Adolescent - emotional problem
Adolescent - emotional problem 		1 0 1 7.1E-02 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 7.1E-02 0 0
CUI: C0393737
Disease: Episodic tension-type headache
Episodic tension-type headache 		1 0 1 7.1E-02 0 0
CUI: C0525046
Disease: Schizophrenia Spectrum and Other Psychotic Disorders
Schizophrenia Spectrum and Other Psychotic Disorders 		1 0 1 7.1E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 7.1E-02 0 0
CUI: C0752147
Disease: Chronic Daily Headache
Chronic Daily Headache 		1 0 1 7.1E-02 0 0
CUI: C0852312
Disease: Gender disorders
Gender disorders 		1 0 1 7.1E-02 0 0
CUI: C1334768
Disease: Minor Salivary Gland Adenocarcinoma
Minor Salivary Gland Adenocarcinoma 		1 0 1 7.1E-02 0 0
CUI: C1335907
Disease: Polymorphous low grade adenocarcinoma of salivary gland
Polymorphous low grade adenocarcinoma of salivary gland 		1 0 1 7.1E-02 0 0
CUI: C1536087
Disease: Negative myoclonus
Negative myoclonus 		1 0 1 7.1E-02 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 7.1E-02 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 7.1E-02 0 0
CUI: C1834559
Disease: Continuous Muscle Fiber Activity, Hereditary
Continuous Muscle Fiber Activity, Hereditary 		1 0 1 7.1E-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 7.1E-02 0 0
CUI: C1838049
Disease: Epilepsy, Nocturnal Frontal Lobe, Type 1
Epilepsy, Nocturnal Frontal Lobe, Type 1 		1 0 1 7.1E-02 0 0
CUI: C1847360
Disease: PARKINSON DISEASE 10
PARKINSON DISEASE 10 		1 0 1 7.1E-02 0 0
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 7.1E-02 0 0
CUI: C1970270
Disease: Choreoathetosis And Congenital Hypothyroidism
Choreoathetosis And Congenital Hypothyroidism 		1 0 1 7.1E-02 0 0
CUI: C2674766
Disease: Myokymia 1
Myokymia 1 		1 0 1 7.1E-02 0 0
CUI: C2677106
Disease: Atrial Fibrillation, Familial, 7
Atrial Fibrillation, Familial, 7 		1 0 1 7.1E-02 0 0