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: C1836076
Disease: Amyotrophic Lateral Sclerosis, Chmp2B-Related
Amyotrophic Lateral Sclerosis, Chmp2B-Related 		1 0 1 0.33 0 0
CUI: C3275487
Disease: X-linked cerebral, cerebellar, coloboma syndrome
X-linked cerebral, cerebellar, coloboma syndrome 		1 0 1 0.33 0 0
CUI: C0231221
Disease: Asymptomatic
Asymptomatic 		2 0 1 0.25 0 0
CUI: C1969722
Disease: Impaired pursuit initiation and maintenance
Impaired pursuit initiation and maintenance 		2 0 1 0.25 0 0
CUI: C4023053
Disease: Cerebellar Purkinje layer atrophy
Cerebellar Purkinje layer atrophy 		2 0 1 0.25 0 0
CUI: C3662068
Disease: Static encephalopathy
Static encephalopathy 		3 0 1 0.20 0 0
CUI: C4022785
Disease: Iron accumulation in substantia nigra
Iron accumulation in substantia nigra 		3 0 1 0.20 0 0
CUI: C2673913
Disease: Anemia, Hypochromic Microcytic, With Iron Overload
Anemia, Hypochromic Microcytic, With Iron Overload 		4 0 1 0.17 0 0
CUI: C3826102
Disease: Iron deficiency anemia in children
Iron deficiency anemia in children 		4 0 1 0.17 0 0
CUI: C1833296
Disease: FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED
FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED 		6 0 1 0.12 0 0
CUI: C1370723
Disease: Stromal sarcoma
Stromal sarcoma 		7 0 1 0.11 0 0
CUI: C0003113
Disease: Anomia
Anomia 		8 0 1 1.0E-01 0 0
CUI: C0234502
Disease: Visual Agnosia
Visual Agnosia 		8 0 1 1.0E-01 0 0
CUI: C0948120
Disease: Hepatic siderosis
Hepatic siderosis 		8 0 1 1.0E-01 0 0
CUI: C3550973
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5 		19 0 2 1.0E-01 0 0
CUI: C4072928
Disease: Spoken Word Recognition Deficit
Spoken Word Recognition Deficit 		8 0 1 1.0E-01 0 0
CUI: C0002018
Disease: Alexia
Alexia 		9 0 1 9.1E-02 0 0
CUI: C0919974
Disease: Abulia
Abulia 		9 0 1 9.1E-02 0 0
CUI: C1838320
Disease: Hyperorality
Hyperorality 		10 0 1 8.3E-02 0 0
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 0 1 8.3E-02 0 0
CUI: C4023470
Disease: EEG with continuous slow activity
EEG with continuous slow activity 		10 0 1 8.3E-02 0 0
CUI: C4024956
Disease: Grammar-specific speech disorder
Grammar-specific speech disorder 		10 0 1 8.3E-02 0 0
CUI: C0003550
Disease: Broca Aphasia
Broca Aphasia 		11 0 1 7.7E-02 0 0
CUI: C0393584
Disease: Benign Hereditary Chorea
Benign Hereditary Chorea 		13 0 1 6.7E-02 0 0
CUI: C3888102
Disease: Frontotemporal Dementia With Motor Neuron Disease
Frontotemporal Dementia With Motor Neuron Disease 		13 0 1 6.7E-02 0 0