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: C0034350
Disease: Pyruvate Metabolism, Inborn Errors
Pyruvate Metabolism, Inborn Errors 		1 0 1 2.8E-02 0 0
CUI: C0154674
Disease: Symptomatic torsion dystonia
Symptomatic torsion dystonia 		1 0 1 2.8E-02 0 0
CUI: C0154675
Disease: Fragments of torsion dystonia
Fragments of torsion dystonia 		1 0 1 2.8E-02 0 0
CUI: C0238014
Disease: Acute cerebellar ataxia
Acute cerebellar ataxia 		1 0 1 2.8E-02 0 0
CUI: C0338483
Disease: Migraine with Prolonged Aura
Migraine with Prolonged Aura 		1 0 1 2.8E-02 0 0
CUI: C0341266
Disease: Diverticulosis of the duodenum
Diverticulosis of the duodenum 		1 0 1 2.8E-02 0 0
CUI: C0393601
Disease: Idiopathic non-familial dystonia
Idiopathic non-familial dystonia 		1 0 1 2.8E-02 0 0
CUI: C0477360
Disease: Other dystonia
Other dystonia 		1 0 1 2.8E-02 0 0
CUI: C0576690
Disease: Impaired body position sense
Impaired body position sense 		1 0 1 2.8E-02 0 0
CUI: C0581882
Disease: Transient neurological symptoms
Transient neurological symptoms 		1 0 1 2.8E-02 0 0
CUI: C0598121
Disease: Hypoglycorrhachia
Hypoglycorrhachia 		1 0 1 2.8E-02 0 0
CUI: C0796124
Disease: Proud Syndrome
Proud Syndrome 		1 0 1 2.8E-02 0 0
CUI: C1719382
Disease: Acquired torsion dystonia
Acquired torsion dystonia 		1 0 1 2.8E-02 0 0
CUI: C1832855
Disease: CHOREOATHETOSIS/SPASTICITY, EPISODIC
CHOREOATHETOSIS/SPASTICITY, EPISODIC 		1 0 1 2.8E-02 0 0
CUI: C1832885
Disease: MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA
MIGRAINE, SPORADIC HEMIPLEGIC, WITH PROGRESSIVE CEREBELLAR ATAXIA 		1 0 1 2.8E-02 0 0
CUI: C1834559
Disease: Continuous Muscle Fiber Activity, Hereditary
Continuous Muscle Fiber Activity, Hereditary 		1 0 1 2.8E-02 0 0
CUI: C1836383
Disease: SPINOCEREBELLAR ATAXIA 27
SPINOCEREBELLAR ATAXIA 27 		1 0 1 2.8E-02 0 0
CUI: C1836439
Disease: Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 		1 0 1 2.8E-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 2.8E-02 0 0
CUI: C1839565
Disease: Optic Atrophy Spastic Paraplegia Syndrome
Optic Atrophy Spastic Paraplegia Syndrome 		1 0 1 2.8E-02 0 0
CUI: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3 		1 0 1 2.8E-02 0 0
CUI: C1846171
Disease: Lissencephaly, X-Linked, 2
Lissencephaly, X-Linked, 2 		1 0 1 2.8E-02 0 0
CUI: C1846172
Disease: Hydranencephaly and Abnormal Genitalia
Hydranencephaly and Abnormal Genitalia 		1 0 1 2.8E-02 0 0
CUI: C1847507
Disease: Paroxysmal lethargy
Paroxysmal lethargy 		1 0 1 2.8E-02 0 0
CUI: C1856194
Disease: Neutral hyperaminoaciduria
Neutral hyperaminoaciduria 		1 0 1 2.8E-02 0 0