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: C0234509
Disease: Finger Agnosia
Finger Agnosia
7 0 7 0.37 0 0
Deposits immunoreactive to beta-amyloid protein
8 0 7 0.35 0 0
CUI: C1838604
Disease: EPILEPSY, CHILDHOOD ABSENCE, 1
EPILEPSY, CHILDHOOD ABSENCE, 1
6 0 6 0.32 0 0
EEG with spike-wave complexes (2.5-3.5 Hz)
6 0 6 0.32 0 0
CUI: C1854686
Disease: Uncontrolled eye movements
Uncontrolled eye movements
7 0 6 0.30 0 0
CUI: C1963933
Disease: Punding
Punding
7 0 6 0.30 0 0
CUI: C0679136
Disease: Low self-esteem
Low self-esteem
10 0 6 0.26 0 0
CUI: C1855568
Disease: Jerky head movements
Jerky head movements
10 0 6 0.26 0 0
CUI: C0338462
Disease: Semantic Dementia
Semantic Dementia
20 0 7 0.22 0 0
Impaired visuospatial constructive cognition
15 0 6 0.21 0 0
CUI: C4477055
Disease: Limb myoclonus
Limb myoclonus
15 0 6 0.21 0 0
Neurofibrillary degeneration (morphologic abnormality)
21 0 7 0.21 0 0
CUI: C0234410
Disease: Physiologic disinhibition
Physiologic disinhibition
23 0 7 0.20 0 0
CUI: C0020578
Disease: Hyperventilation
Hyperventilation
31 0 6 0.14 0 0
CUI: C0001890
Disease: Akinetic Petit Mal
Akinetic Petit Mal
7 0 3 0.13 0 0
CUI: C4281785
Disease: Childhood Absence Epilepsy
Childhood Absence Epilepsy
33 0 6 0.13 0 0
CUI: C4553705
Disease: Absence Seizure Disorder
Absence Seizure Disorder
7 0 3 0.13 0 0
CUI: C0234144
Disease: Dysgraphia
Dysgraphia
43 0 7 0.13 0 0
CUI: C0751124
Disease: Epilepsy, Absence, Atypical
Epilepsy, Absence, Atypical
8 0 3 0.12 0 0
CUI: C4552765
Disease: Epilepsy, Minor
Epilepsy, Minor
8 0 3 0.12 0 0
CUI: C0751071
Disease: Familial Dementia
Familial Dementia
18 0 4 0.12 0 0
CUI: C4505072
Disease: Epileptic Syndromes
Epileptic Syndromes
46 0 7 0.12 0 0
CUI: C0349081
Disease: Dementia in Parkinson's disease
Dementia in Parkinson's disease
9 0 3 0.12 0 0
CUI: C2931784
Disease: Amyloid angiopathy
Amyloid angiopathy
9 0 3 0.12 0 0
CUI: C0233407
Disease: Disorientation
Disorientation
12 0 3 0.11 0 0