Preferred Label : cerebral amyloid angiopathy, familial;
MeSH definition : A familial disorder marked by AMYLOID deposits in the walls of small and medium sized
blood vessels of CEREBRAL CORTEX and MENINGES.;
MeSH synonym : familial cerebral amyloid angiopathy; autosomal dominant cerebrovascular amyloidosis; HCHWA;
CISMeF synonym : dutch type hereditary cerebral amyloid angiopathy;
MeSH hyponym : cerebral amyloid angiopathy, genetic; hereditary cerebral amyloid angiopathy, icelandic type; hereditary cerebral amyloid angiopathy, dutch type; cerebral amyloid angiopathy, hereditary; Icelandic Type Hereditary Cerebral Amyloid Angiopathy; Cerebral Amyloid Angiopathy, Cst3-Related; Cerebral Amyloid Angiopathy, Cst3 Related; Icelandic Type Amyloidosis; Amyloidosis, Icelandic Type; Amyloidosis VI; Amyloidosis VIs; Amyloidosis, Cerebroarterial, Icelandic Type; Hereditary Cerebral Amyloid Angiopathy; Hereditary Cerebral Hemorrhage With Amyloidosis; Cerebral Hemorrhage, Hereditary, With Amyloidosis;
Origin ID : D028243;
UMLS CUI : C0268393;
- Allowable qualifiers
- Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
- DO Cross reference
- ORDO relation(s)
- Record concept(s)
- Related MeSH Supplementary Concept(s)
- See also (suggested by CISMeF)
- Semantic type(s)
A familial disorder marked by AMYLOID deposits in the walls of small and medium sized
blood vessels of CEREBRAL CORTEX and MENINGES.