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: C0270726
Disease: Alexander Disease
Alexander Disease 		27 0 10 1.0E-01 0 0
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease 		186 52 24 9.8E-02 1 1.4E-02
CUI: C3825201
Disease: Mitochondrial pathology
Mitochondrial pathology 		20 6 9 9.6E-02 1 4.0E-02
CUI: C0037763
Disease: Spasm
Spasm 		172 0 22 9.4E-02 0 0
CUI: C1839780
Disease: FRAGILE X TREMOR/ATAXIA SYNDROME
FRAGILE X TREMOR/ATAXIA SYNDROME 		62 0 12 9.0E-02 0 0
CUI: C0522224
Disease: Paralysed
Paralysed 		68 0 12 8.6E-02 0 0
CUI: C2718017
Disease: TDP-43 Proteinopathies
TDP-43 Proteinopathies 		44 0 10 8.5E-02 0 0
CUI: C1832370
Disease: MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED
MYOPATHY, MYOFIBRILLAR, DESMIN-RELATED 		20 0 8 8.4E-02 0 0
CUI: C3811918
Disease: GRN-related frontotemporal dementia
GRN-related frontotemporal dementia 		112 20 15 8.3E-02 2 5.3E-02
CUI: C1708350
Disease: Hereditary Leiomyomatosis and Renal Cell Cancer
Hereditary Leiomyomatosis and Renal Cell Cancer 		61 0 11 8.3E-02 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 8 8.2E-02 0 0
CUI: C0740447
Disease: Diabetic peripheral neuropathy
Diabetic peripheral neuropathy 		129 0 16 8.2E-02 0 0
CUI: C3888102
Disease: Frontotemporal Dementia With Motor Neuron Disease
Frontotemporal Dementia With Motor Neuron Disease 		13 0 7 7.9E-02 0 0
CUI: C4024896
Disease: Motor neuron atrophy
Motor neuron atrophy 		138 21 16 7.8E-02 1 2.5E-02
CUI: C0333440
Disease: Hyaline body
Hyaline body 		14 0 7 7.8E-02 0 0
CUI: C0270790
Disease: Quadriparesis
Quadriparesis 		42 0 9 7.8E-02 0 0
CUI: C0424296
Disease: Social disinhibition
Social disinhibition 		56 0 10 7.8E-02 0 0
CUI: C0272401
Disease: Virchow's node (disorder)
Virchow's node (disorder) 		30 1 8 7.6E-02 1 5.0E-02
CUI: C0238190
Disease: Inclusion Body Myositis (disorder)
Inclusion Body Myositis (disorder) 		87 0 12 7.6E-02 0 0
CUI: C1963060
Disease: Agitation, CTCAE 3.0
Agitation, CTCAE 3.0 		87 0 12 7.6E-02 0 0
CUI: C4552855
Disease: Agitation, CTCAE 5.0
Agitation, CTCAE 5.0 		87 0 12 7.6E-02 0 0
CUI: C0949664
Disease: Tauopathies
Tauopathies 		245 43 23 7.5E-02 3 5.0E-02
CUI: C1285162
Disease: Degenerative disorder
Degenerative disorder 		160 0 17 7.5E-02 0 0
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
Parkinson Disease, Familial, Type 1 		46 27 9 7.5E-02 2 4.4E-02
CUI: C1838244
Disease: TIBIAL MUSCULAR DYSTROPHY, TARDIVE
TIBIAL MUSCULAR DYSTROPHY, TARDIVE 		18 0 7 7.4E-02 0 0