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: C0024408
Disease: Machado-Joseph Disease
Machado-Joseph Disease 		135 0 15 7.4E-02 0 0
CUI: C4082299
Disease: Bulbar palsy
Bulbar palsy 		48 0 9 7.4E-02 0 0
CUI: C0027746
Disease: Nerve Degeneration
Nerve Degeneration 		165 0 17 7.4E-02 0 0
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration 		195 54 19 7.3E-02 2 2.8E-02
CUI: C0235025
Disease: Peripheral motor neuropathy
Peripheral motor neuropathy 		64 0 10 7.3E-02 0 0
CUI: C0869474
Disease: Dyscalculia
Dyscalculia 		20 0 7 7.3E-02 0 0
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked 		126 0 14 7.2E-02 0 0
CUI: C0085632
Disease: Apathy
Apathy 		83 9 11 7.1E-02 1 3.6E-02
CUI: C0156149
Disease: Gastrointestinal tract vascular insufficiency
Gastrointestinal tract vascular insufficiency 		68 0 10 7.1E-02 0 0
CUI: C2004435
Disease: Vascular insufficiency of intestine
Vascular insufficiency of intestine 		68 0 10 7.1E-02 0 0
CUI: C0751713
Disease: Inclusion Body Myopathy, Sporadic
Inclusion Body Myopathy, Sporadic 		84 0 11 7.1E-02 0 0
CUI: C1257763
Disease: Overnutrition
Overnutrition 		54 0 9 7.0E-02 0 0
CUI: C0426980
Disease: Motor symptoms
Motor symptoms 		100 15 12 7.0E-02 4 0.13
CUI: C0039496
Disease: Temporomandibular Joint Dysfunction Syndrome
Temporomandibular Joint Dysfunction Syndrome 		24 0 7 7.0E-02 0 0
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases 		284 84 24 7.0E-02 1 9.7E-03
CUI: C4552811
Disease: Generalized Muscle Weakness, CTCAE
Generalized Muscle Weakness, CTCAE 		117 0 13 7.0E-02 0 0
CUI: C1859807
Disease: AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE (disorder) 		25 0 7 6.9E-02 0 0
CUI: C0029401
Disease: Osteitis Deformans
Osteitis Deformans 		134 0 14 6.9E-02 0 0
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy 		41 0 8 6.9E-02 0 0
CUI: C0752304
Disease: Hypoxic-Ischemic Encephalopathy
Hypoxic-Ischemic Encephalopathy 		182 0 17 6.9E-02 0 0
CUI: C1863843
Disease: Neuronal intranuclear inclusion disease
Neuronal intranuclear inclusion disease 		12 0 6 6.7E-02 0 0
CUI: C0085631
Disease: Agitation
Agitation 		109 0 12 6.7E-02 0 0
CUI: C4014650
Disease: Abnormal mitochondrial morphology
Abnormal mitochondrial morphology 		13 0 6 6.7E-02 0 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		126 0 13 6.6E-02 0 0
CUI: C0162671
Disease: MELAS Syndrome
MELAS Syndrome 		80 0 10 6.5E-02 0 0