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: C0454596
Disease: Dysarthria, Spastic
Dysarthria, Spastic 		30 0 4 8.0E-02 0 0
CUI: C4302342
Disease: Familial hemolytic uremic syndrome
Familial hemolytic uremic syndrome 		3 0 2 8.0E-02 0 0
CUI: C0032027
Disease: Pityriasis Rubra Pilaris
Pityriasis Rubra Pilaris 		32 0 4 7.7E-02 0 0
CUI: C0238651
Disease: Ankle clonus
Ankle clonus 		32 0 4 7.7E-02 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia 		18 0 3 7.7E-02 0 0
CUI: C4021577
Disease: Abnormality of somatosensory evoked potentials
Abnormality of somatosensory evoked potentials 		4 0 2 7.7E-02 0 0
CUI: C4025614
Disease: EMG: chronic denervation signs
EMG: chronic denervation signs 		18 0 3 7.7E-02 0 0
CUI: C0009676
Disease: Confusion
Confusion 		75 0 7 7.6E-02 0 0
CUI: C1856507
Disease: Bulbar signs
Bulbar signs 		33 0 4 7.5E-02 0 0
CUI: C1720037
Disease: Supranuclear gaze palsy
Supranuclear gaze palsy 		19 0 3 7.5E-02 0 0
CUI: C0231690
Disease: Titubation
Titubation 		5 0 2 7.4E-02 0 0
CUI: C0542141
Disease: Paralysis radial
Paralysis radial 		5 0 2 7.4E-02 0 0
CUI: C0852996
Disease: Progressive cerebellar degeneration
Progressive cerebellar degeneration 		5 0 2 7.4E-02 0 0
CUI: C1306600
Disease: Radial nerve palsy
Radial nerve palsy 		5 0 2 7.4E-02 0 0
CUI: C4025720
Disease: Pseudobulbar behavioral symptoms
Pseudobulbar behavioral symptoms 		5 0 2 7.4E-02 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia 		20 0 3 7.3E-02 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary 		35 3 4 7.3E-02 1 0.14
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases 		66 4 6 7.1E-02 1 0.12
CUI: C0338582
Disease: Sporadic Cerebral Amyloid Angiopathy
Sporadic Cerebral Amyloid Angiopathy 		6 0 2 7.1E-02 0 0
CUI: C1865322
Disease: MIGRAINE, FAMILIAL HEMIPLEGIC, 2
MIGRAINE, FAMILIAL HEMIPLEGIC, 2 		6 14 2 7.1E-02 1 5.6E-02
CUI: C2677567
Disease: DYSTONIA 16 (disorder)
DYSTONIA 16 (disorder) 		6 0 2 7.1E-02 0 0
CUI: C3854629
Disease: Tendon thickening
Tendon thickening 		6 0 2 7.1E-02 0 0
CUI: C0542223
Disease: Loss of speech
Loss of speech 		37 0 4 7.0E-02 0 0
CUI: C0751254
Disease: Creutzfeldt-Jakob Disease, Familial
Creutzfeldt-Jakob Disease, Familial 		22 0 3 7.0E-02 0 0
CUI: C0234509
Disease: Finger Agnosia
Finger Agnosia 		7 0 2 6.9E-02 0 0