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: C0038220
Disease: Status Epilepticus
Status Epilepticus 		533 12 76 8.5E-02 1 7.6E-03
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		1114 485 120 8.4E-02 1 1.7E-03
CUI: C0752125
Disease: Spinocerebellar Ataxia Type 7
Spinocerebellar Ataxia Type 7 		78 0 40 8.4E-02 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady 		143 14 45 8.3E-02 1 7.5E-03
CUI: C0151786
Disease: Muscle Weakness
Muscle Weakness 		536 87 75 8.3E-02 3 1.5E-02
CUI: C0008489
Disease: Chorea
Chorea 		168 0 46 8.2E-02 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		568 51 76 8.1E-02 4 2.4E-02
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases 		66 4 38 8.1E-02 3 2.5E-02
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		213 0 49 8.1E-02 0 0
CUI: C0026837
Disease: Muscle Rigidity
Muscle Rigidity 		320 25 57 8.1E-02 1 6.9E-03
CUI: C0024408
Disease: Machado-Joseph Disease
Machado-Joseph Disease 		135 0 43 8.1E-02 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 45 8.0E-02 0 0
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		2165 159 193 8.0E-02 3 1.1E-02
CUI: C0020179
Disease: Huntington Disease
Huntington Disease 		978 115 105 8.0E-02 1 4.3E-03
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders 		607 0 77 7.9E-02 0 0
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		1263 112 124 7.8E-02 1 4.3E-03
CUI: C0234979
Disease: Dysdiadochokinesis
Dysdiadochokinesis 		49 7 35 7.7E-02 3 2.4E-02
CUI: C1112256
Disease: Sensorimotor neuropathy
Sensorimotor neuropathy 		93 21 38 7.7E-02 2 1.4E-02
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		967 579 100 7.6E-02 8 1.2E-02
CUI: C0949664
Disease: Tauopathies
Tauopathies 		245 0 48 7.5E-02 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation 		505 98 66 7.5E-02 2 9.3E-03
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 41 39 7.4E-02 1 6.3E-03
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
Henoch-Schoenlein Purpura 		198 59 44 7.4E-02 2 1.1E-02
CUI: C0004135
Disease: Ataxia Telangiectasia
Ataxia Telangiectasia 		384 698 56 7.3E-02 1 1.2E-03
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		312 23 51 7.3E-02 1 7.0E-03