cerebral amyloid angiopathy, APP-related
Also known as HCHWAD, amyloidosis, Cerebroarterial, APP-related, cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants, APP-related cerebral amyloid angiopathy+6 more
HCHWAD, amyloidosis, Cerebroarterial, APP-related, cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants, APP-related cerebral amyloid angiopathy, amyloidosis, hereditary, with cerebral hemorrhage, Dutch variant, cerebral amyloid angiopathy, APP-related, Arctic variant, cerebral amyloid angiopathy, APP-related, Dutch variant, cerebral amyloid angiopathy, APP-related, Flemish variant, cerebral amyloid angiopathy, APP-related, Iowa variant, cerebral amyloid angiopathy, APP-related, Italian variant.
What's happening now
An analyst briefing on current research, clinical, regulatory and industry activity surrounding this disease.
Associated genes
Genes associated with this disease in the canonical knowledge graph (Open Targets evidence). Number shows the association score.
Disease biology
Proteins whose encoding gene is associated with this disease, reached through the canonical gene→disease graph. Number shows the gene's association score.
Reference
Authoritative identity, definition & identifiers.
HCHWAD, amyloidosis, Cerebroarterial, APP-related, cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants, APP-related cerebral amyloid angiopathy, amyloidosis, hereditary, with cerebral hemorrhage, Dutch variant, cerebral amyloid angiopathy, APP-related, Arctic variant, cerebral amyloid angiopathy, APP-related, Dutch variant, cerebral amyloid angiopathy, APP-related, Flemish variant, cerebral amyloid angiopathy, APP-related, Iowa variant, cerebral amyloid angiopathy, APP-related, Italian variant
- Disease identity & definition — NLM Medical Subject Headings (MeSH), public domain
- Related entities are derived from literature co-mention (studied together) — associative, not causal.