ABetaA21G amyloidosis
MONDO:0017948Mondo
Findings
No curated finding names ABetaA21G amyloidosis yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Flemish type is a form of HCHWA characterized by an age of onset of 45 years of age, progressive Alzheimer's disease-like dementia and lobar intracerebral hemorrhage in some patients.
Definition from the Mondo Disease Ontology (MONDO:0017948), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- APPHGNC:620
- Supportive · Orphanet · Autosomal dominant · 2021
Where it sits
Other names
6 names
Resolves to: ABetaA21G amyloidosis
- Also called
- ABeta amyloidosis, Flemish typeABetaA21G-related amyloidosiscerebral amyloid angiopathy, APP-related, Flemish variantHCHWA, Flemish typehereditary cerebral haemorrhage with amyloidosis, Flemish typehereditary cerebral hemorrhage with amyloidosis, Flemish type