Cerebral amyloid angiopathy

Disease Term Disease ID Gene Symbol Classification References Source
ABeta amyloidosis, Arctic type 324723 APP Causal Pathogenic evidence from ClinVar - ClinVar
ABeta amyloidosis, Dutch type 100006 APP Causal Pathogenic evidence from ClinVar - ClinVar
ABeta amyloidosis, Iowa type 324708 APP Causal Pathogenic evidence from ClinVar - ClinVar
ABeta amyloidosis, Italian type 324713 APP Causal Pathogenic evidence from ClinVar - ClinVar
ABetaA21G amyloidosis 324718 APP Causal Pathogenic evidence from ClinVar - ClinVar
ABetaL34V amyloidosis 324703 APP Causal Pathogenic evidence from ClinVar - ClinVar
Cerebral Amyloid Angiopathy C0085220 APP Causal Pathogenic evidence from ClinVar 21520056 ClinVar
ITM2B Causal Pathogenic evidence from ClinVar - ClinVar
APOE Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 11061249, 29458411 -
CST3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
HDAC9 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 29458411 -
NECTIN2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 25188341 -
PSEN2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
TRAPPC12 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 29458411 -
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED C2751536 APP Causal Pathogenic evidence from ClinVar 2111584, 10821838, 11409420, 12654973, 16178030, 20228223, 20697050 ClinVar
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ARCTIC VARIANT C2751494 APP Causal Pathogenic evidence from ClinVar 2111584, 10821838 ClinVar
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, FLEMISH VARIANT C3888307 APP Causal Pathogenic evidence from ClinVar 2111584, 10821838 ClinVar
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, IOWA VARIANT C3888309 APP Causal Pathogenic evidence from ClinVar 2111584, 10821838 ClinVar
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, ITALIAN VARIANT C3888308 APP Causal Pathogenic evidence from ClinVar 2111584, 10821838 ClinVar
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type C2931672 APP Causal Pathogenic evidence from ClinVar 2111584, 10821838, 24870607 ClinVar
Sporadic Cerebral Amyloid Angiopathy C0338582 APP Causal Pathogenic evidence from ClinVar 21520056 ClinVar
APOE Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 11061249 -
ABri amyloidosis 97345 ITM2B Causal Pathogenic evidence from ClinVar - ClinVar
CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1 C1867773 ITM2B Causal Pathogenic evidence from ClinVar 10391242, 10781099 ClinVar
CEREBRAL AMYLOID ANGIOPATHY, PRNP-RELATED C3805618 PRNP Causal Pathogenic evidence from ClinVar - ClinVar
Cerebral Amyloid Angiopathy, Genetic C1956349 CST3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 18566660 -
Cerebral Amyloid Angiopathy, Hereditary C1510489 CST3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 18566660 -
Familial Cerebral Amyloid Angiopathy C0268393 CST3 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 18566660 -
Cerebral Amyloid Angiopathy, Gsn-Related C2751493 GSN Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -