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: C2931784
Disease: Amyloid angiopathy
Amyloid angiopathy
9 0 5 0.36 0 0
Deficit in phonologic short-term memory
5 0 3 0.25 0 0
CUI: C1861735
Disease: Dementia, familial Danish
Dementia, familial Danish
10 0 4 0.25 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia
18 0 5 0.22 0 0
Familial encephalopathy with neuroserpin inclusion bodies
7 0 3 0.21 0 0
Familial Alzheimer's disease of early onset
14 0 4 0.20 0 0
CUI: C0520789
Disease: Progressive subcortical gliosis
Progressive subcortical gliosis
2 0 2 0.20 0 0
Cerebral Amyloid Angiopathy, Genetic
2 0 2 0.20 0 0
Neurofibrillary degeneration (morphologic abnormality)
21 0 5 0.19 0 0
CUI: C0349081
Disease: Dementia in Parkinson's disease
Dementia in Parkinson's disease
9 0 3 0.19 0 0
CUI: C0474420
Disease: Inappropriate sexual behavior
Inappropriate sexual behavior
3 0 2 0.18 0 0
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
3 0 2 0.18 0 0
CUI: C4022574
Disease: Limb apraxia
Limb apraxia
3 0 2 0.18 0 0
CUI: C0262424
Disease: CNS DEGENERATION
CNS DEGENERATION
4 0 2 0.17 0 0
CUI: C0520716
Disease: Pallidopontonigral degeneration
Pallidopontonigral degeneration
4 0 2 0.17 0 0
Progressive extrapyramidal muscular rigidity
4 0 2 0.17 0 0
CUI: C4477086
Disease: Cotton wool plaques
Cotton wool plaques
4 0 2 0.17 0 0
CUI: C0740340
Disease: Amyloidosis, Familial
Amyloidosis, Familial
19 0 4 0.16 0 0
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia
20 0 4 0.15 0 0
CUI: C0521175
Disease: Neuropil Threads
Neuropil Threads
13 0 3 0.15 0 0
Sporadic Cerebral Amyloid Angiopathy
6 0 2 0.14 0 0
CUI: C1862968
Disease: Generalized amyloid deposition
Generalized amyloid deposition
6 0 2 0.14 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
23 0 4 0.14 0 0
CUI: C0234509
Disease: Finger Agnosia
Finger Agnosia
7 0 2 0.13 0 0
CUI: C0424304
Disease: Inappropriate laughter
Inappropriate laughter
7 0 2 0.13 0 0