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: C3494934
Disease: Benign paroxysmal torticollis of infancy
Benign paroxysmal torticollis of infancy 		1 0 1 3.8E-02 0 0
CUI: C3714927
Disease: MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO
MULTIPLE SYSTEM ATROPHY 1, SUSCEPTIBILITY TO 		1 0 1 3.8E-02 0 0
CUI: C3809327
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 14 		1 0 1 3.8E-02 0 0
CUI: C4015505
Disease: SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 18 		1 0 1 3.8E-02 0 0
CUI: C4015519
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 28 		1 0 1 3.8E-02 0 0
CUI: C4016431
Disease: CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH QUADRUPEDAL LOCOMOTION 1
CEREBELLAR ATAXIA AND MENTAL RETARDATION WITH QUADRUPEDAL LOCOMOTION 1 		1 0 1 3.8E-02 0 0
CUI: C4016713
Disease: EPISODIC ATAXIA, TYPE 2, AND EPILEPSY
EPISODIC ATAXIA, TYPE 2, AND EPILEPSY 		1 0 1 3.8E-02 0 0
CUI: C4020920
Disease: Enlarged interhemispheric fissure
Enlarged interhemispheric fissure 		1 0 1 3.8E-02 0 0
CUI: C4021571
Disease: Abnormal vestibulo-ocular reflex
Abnormal vestibulo-ocular reflex 		1 0 1 3.8E-02 0 0
CUI: C4022677
Disease: Female anorgasmia
Female anorgasmia 		1 0 1 3.8E-02 0 0
CUI: C4024953
Disease: Dorsal column degeneration
Dorsal column degeneration 		1 0 1 3.8E-02 0 0
CUI: C4225253
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2X 		1 0 1 3.8E-02 0 0
CUI: C4285893
Disease: Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome 		1 0 1 3.8E-02 0 0
CUI: C4310716
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 42 		1 0 1 3.8E-02 0 0
CUI: C4324342
Disease: Dysarthrophonia
Dysarthrophonia 		1 0 1 3.8E-02 0 0
CUI: C4706415
Disease: Spectrin-associated autosomal recessive cerebellar ataxia
Spectrin-associated autosomal recessive cerebellar ataxia 		1 0 1 3.8E-02 0 0
CUI: C4748158
Disease: SPINOCEREBELLAR ATAXIA 48
SPINOCEREBELLAR ATAXIA 48 		1 0 1 3.8E-02 0 0
CUI: C4749507
Disease: 5p13 microduplication syndrome
5p13 microduplication syndrome 		1 0 1 3.8E-02 0 0
CUI: C4749578
Disease: Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency 		1 0 1 3.8E-02 0 0
CUI: C0024528
Disease: Malaise and fatigue
Malaise and fatigue 		2 0 1 3.7E-02 0 0
CUI: C0152236
Disease: Talipes valgus
Talipes valgus 		2 0 1 3.7E-02 0 0
CUI: C0268632
Disease: Homocarnosinosis
Homocarnosinosis 		2 0 1 3.7E-02 0 0
CUI: C0477373
Disease: Other forms of migraine
Other forms of migraine 		2 0 1 3.7E-02 0 0
CUI: C0494479
Disease: Other headache syndrome
Other headache syndrome 		2 0 1 3.7E-02 0 0
CUI: C0749201
Disease: Orthostatic syncope
Orthostatic syncope 		2 0 1 3.7E-02 0 0