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: C0338582
Disease: Sporadic Cerebral Amyloid Angiopathy
Sporadic Cerebral Amyloid Angiopathy 		6 0 4 0.36 0 0
CUI: C1867773
Disease: CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1
CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1 		10 0 5 0.36 0 0
CUI: C0338445
Disease: Familial Alzheimer's disease of early onset
Familial Alzheimer's disease of early onset 		14 33 6 0.35 1 2.9E-02
CUI: C0349081
Disease: Dementia in Parkinson's disease
Dementia in Parkinson's disease 		9 0 4 0.29 0 0
CUI: C0268392
Disease: Localized amyloidosis
Localized amyloidosis 		5 0 3 0.27 0 0
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia 		20 0 6 0.26 0 0
CUI: C0234509
Disease: Finger Agnosia
Finger Agnosia 		7 0 3 0.23 0 0
CUI: C1858680
Disease: Familial encephalopathy with neuroserpin inclusion bodies
Familial encephalopathy with neuroserpin inclusion bodies 		7 0 3 0.23 0 0
CUI: C0338460
Disease: Argyrophilic grain disease
Argyrophilic grain disease 		18 0 5 0.23 0 0
CUI: C1847200
Disease: ALZHEIMER DISEASE 4
ALZHEIMER DISEASE 4 		2 13 2 0.22 1 6.7E-02
CUI: C0003113
Disease: Anomia
Anomia 		8 0 3 0.21 0 0
CUI: C1853934
Disease: Deposits immunoreactive to beta-amyloid protein
Deposits immunoreactive to beta-amyloid protein 		8 0 3 0.21 0 0
CUI: C2931672
Disease: Cerebral hemorrhage with amyloidosis, hereditary, Dutch type
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type 		20 0 5 0.21 0 0
CUI: C0085400
Disease: Neurofibrillary degeneration (morphologic abnormality)
Neurofibrillary degeneration (morphologic abnormality) 		21 0 5 0.20 0 0
CUI: C0474420
Disease: Inappropriate sexual behavior
Inappropriate sexual behavior 		3 0 2 0.20 0 0
CUI: C1527338
Disease: Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type 		3 0 2 0.20 0 0
CUI: C4022574
Disease: Limb apraxia
Limb apraxia 		3 0 2 0.20 0 0
CUI: C4022794
Disease: Parietal hypometabolism in FDG PET
Parietal hypometabolism in FDG PET 		3 0 2 0.20 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition 		23 0 5 0.19 0 0
CUI: C0520574
Disease: Cerebrovascular amyloidosis
Cerebrovascular amyloidosis 		4 0 2 0.18 0 0
CUI: C0520716
Disease: Pallidopontonigral degeneration
Pallidopontonigral degeneration 		4 0 2 0.18 0 0
CUI: C0268393
Disease: Familial Cerebral Amyloid Angiopathy
Familial Cerebral Amyloid Angiopathy 		18 0 4 0.17 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia 		18 0 4 0.17 0 0
CUI: C0233407
Disease: Disorientation
Disorientation 		12 0 3 0.17 0 0
CUI: C1510489
Disease: Cerebral Amyloid Angiopathy, Hereditary
Cerebral Amyloid Angiopathy, Hereditary 		19 4 4 0.17 2 0.40