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EXPERIMENTAL FACTOR ONTOLOGY - ANNOTATIONS

Term:cerebral amyloid angiopathy
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Accession:EFO:0006790 term browser browse the term
Definition:A disorder characterized by the deposition of amyloid in the wall of the vessels in the brain. Hereditary cerebral hemorrhage with amyloidosis (HCHWA) describes a group of rare familial central nervous system disorders characterized by amyloid deposition in the cerebral blood vessels leading to hemorrhagic and non-hemorrhagic strokes, focal neurological deficits, and progressive cognitive decline eventually leading to dementia.
Synonyms:exact_synonym: CAA;   HCHWA;   dutch hereditary cerebral amyloid angiopathy;   hereditary cerebral haemorrhage with amyloidosis - Dutch type;   hereditary cerebral hemorrhage with amyloidosis - Dutch type
 related_synonym: CAA, familial;   cerebral amyloid angiopathy, familial;   cerebral amyloid angiopathy, genetic
 xref: DOID:9246;   GARD:10266;   HP:0011970;   ICD10CM:I68.0;   ICD10EXP:E85.4+;   ICD10EXP:I68.0*;   ICD9:277.39;   MEDGEN:267610;   MESH:D016657;   MONDO:0005620;   MP:0004254;   MedDRA:10068044;   NCI:C84625;   ORDO:85458;   SCTID:230724001;   SNOMEDCT:230724001;   UMLS:C1510489


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Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          genetic disorder 0
            hereditary neurological disease 0
              cerebral amyloid angiopathy 0
                ABri amyloidosis 0
                ACys amyloidosis 0
                ADan amyloidosis 0
                cerebral amyloid angiopathy, APP-related + 0
Path 2
Term Annotations click to browse term
  experimental factor 0
    material property 0
      disposition 0
        disease 0
          nervous system disease 0
            central nervous system disease 0
              brain disease 0
                mental or behavioural disorder 0
                  cerebral amyloid angiopathy 0
                    ABri amyloidosis 0
                    ACys amyloidosis 0
                    ADan amyloidosis 0
                    cerebral amyloid angiopathy, APP-related + 0
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