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: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) 		27 67 26 0.81 51 0.73
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
Amyotrophic Lateral Sclerosis, Sporadic 		173 90 31 0.18 52 0.57
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1 		164 139 31 0.19 53 0.38
CUI: C4509818
Disease: Facial onset sensory and motor neuronopathy syndrome
Facial onset sensory and motor neuronopathy syndrome 		1 1 1 3.2E-02 1 1.9E-02
CUI: C0751401
Disease: Ophthalmoparesis
Ophthalmoparesis 		0 4 0 0 1 1.8E-02
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		1114 485 10 8.8E-03 9 1.7E-02
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
Amyotrophic Lateral Sclerosis, Familial 		130 68 3 1.9E-02 2 1.7E-02
CUI: C0221505
Disease: Lesion of brain
Lesion of brain 		188 9 2 9.2E-03 1 1.6E-02
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked 		126 30 4 2.6E-02 1 1.2E-02
CUI: C0677932
Disease: Progressive Neoplastic Disease
Progressive Neoplastic Disease 		384 40 2 4.8E-03 1 1.1E-02
CUI: C3539781
Disease: Progressive cGVHD
Progressive cGVHD 		384 40 2 4.8E-03 1 1.1E-02
CUI: C0030552
Disease: Paresis
Paresis 		216 49 2 8.2E-03 1 9.8E-03
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy 		176 52 6 3.0E-02 1 9.5E-03
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease 		186 52 7 3.3E-02 1 9.5E-03
CUI: C0162534
Disease: Prion Diseases
Prion Diseases 		175 67 6 3.0E-02 1 8.3E-03
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		508 121 6 1.1E-02 1 5.7E-03
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia 		320 215 7 2.0E-02 1 3.7E-03
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		1075 276 7 6.4E-03 1 3.0E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		1630 348 11 6.7E-03 1 2.5E-03
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		2078 990 8 3.8E-03 2 1.9E-03
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		1800 1022 7 3.8E-03 1 9.3E-04
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 5 4.4E-03 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 1 2.7E-02 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		243 0 2 7.4E-03 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 0 1 6.0E-03 0 0