Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Cerebral Amyloid Angiopathy, Genetic
2 0 2 0.67 0 0
Hereditary cerebrovascular amyloidosis
1 0 1 0.33 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system
1 0 1 0.33 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis
1 0 1 0.33 0 0
Age-Related Macular Degeneration type 11
1 0 1 0.33 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT
1 0 1 0.33 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
1 0 1 0.33 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT
1 0 1 0.33 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT
1 0 1 0.33 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT
1 0 1 0.33 0 0
RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES
1 0 1 0.33 0 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT
1 0 1 0.33 0 0
CUI: C4025264
Disease: Recurrent cerebral hemorrhage
Recurrent cerebral hemorrhage
1 0 1 0.33 0 0
CUI: C0553692
Disease: Brain hemorrhage
Brain hemorrhage
10 0 3 0.30 0 0
CUI: C1861735
Disease: Dementia, familial Danish
Dementia, familial Danish
10 0 3 0.30 0 0
Sporadic Cerebral Amyloid Angiopathy
6 0 2 0.29 0 0
CUI: C0149854
Disease: Cerebellar hemorrhage
Cerebellar hemorrhage
2 0 1 0.25 0 0
CUI: C0600074
Disease: Autotomy
Autotomy
2 0 1 0.25 0 0
Congenital urinary tract obstruction
2 0 1 0.25 0 0
Acute disease of cardiovascular system
2 0 1 0.25 0 0
CUI: C1411876
Disease: Developmental arithmetic disorder
Developmental arithmetic disorder
2 0 1 0.25 0 0
CUI: C1619716
Disease: Cystatin C measurement
Cystatin C measurement
2 0 1 0.25 0 0
CUI: C1836791
Disease: Tortuous cerebral arteries
Tortuous cerebral arteries
2 0 1 0.25 0 0
Primary angiitis of the central nervous system
2 0 1 0.25 0 0
CUI: C4087189
Disease: Locomotive syndrome
Locomotive syndrome
2 0 1 0.25 0 0