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: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease
1 0 1 0.50 0 0
Hereditary cerebrovascular amyloidosis
1 0 1 0.50 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system
1 0 1 0.50 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis
1 0 1 0.50 0 0
Charcot-Marie-Tooth disease, demyelinating, Type 1F
1 0 1 0.50 0 0
CUI: C1843169
Disease: Clusters of axonal regeneration
Clusters of axonal regeneration
1 0 1 0.50 0 0
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)
1 0 1 0.50 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
1 0 1 0.50 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
1 0 1 0.50 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT
1 0 1 0.50 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT
1 0 1 0.50 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT
1 0 1 0.50 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT
1 0 1 0.50 0 0
CUI: C4025264
Disease: Recurrent cerebral hemorrhage
Recurrent cerebral hemorrhage
1 0 1 0.50 0 0
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G
1 0 1 0.50 0 0
Charcot-Marie-Tooth disease type 2B5
1 0 1 0.50 0 0
CUI: C0149854
Disease: Cerebellar hemorrhage
Cerebellar hemorrhage
2 0 1 0.33 0 0
CUI: C0600074
Disease: Autotomy
Autotomy
2 0 1 0.33 0 0
CUI: C1411876
Disease: Developmental arithmetic disorder
Developmental arithmetic disorder
2 0 1 0.33 0 0
CUI: C1836791
Disease: Tortuous cerebral arteries
Tortuous cerebral arteries
2 0 1 0.33 0 0
Hypotrophy of the small hand muscles
2 0 1 0.33 0 0
CUI: C0241832
Disease: Cerebrovascular Insufficiency
Cerebrovascular Insufficiency
3 0 1 0.25 0 0
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
3 0 1 0.25 0 0
Charcot-Marie-Tooth disease, Type 2B1
3 0 1 0.25 0 0
CUI: C2363813
Disease: Short-term memory impairment
Short-term memory impairment
3 0 1 0.25 0 0