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cerebral amyloid angiopathy, APP-related

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Disease Overview

A cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of APP on chromosome 21q21.3.

Synonyms

  • APP-related cerebral amyloid angiopathy
  • HCHWAD
  • amyloidosis, Cerebroarterial, APP-related
  • amyloidosis, hereditary, with cerebral hemorrhage, Dutch variant
  • cerebral amyloid angiopathy, APP-related
  • 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
  • cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants
OMIM

Online Mendelian Inheritance In Man (OMIM) has a summary of published research about this condition and includes references from the medical literature. The summary contains medical and scientific terms, so we encourage you to share and discuss this information with your doctor. OMIM is authored and edited at the McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine.

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MedlinePlus

MedlinePlus has information about this condition that may include a description, frequency, causes, inheritance, and links to more information. The information is written for the public, including patients, caregivers and families. MedlinePlus is a service of the National Library of Medicine (NLM), which is part of the National Institutes of Health (NIH).

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