MeSH Browser

MeSH Heading: Cerebral Amyloid Angiopathy, Familial
Tree Number(s): C10.228.140.163.100.168; C10.228.140.300.275.311; C10.228.140.300.510.200.200.160; C14.907.253.329.311; C14.907.253.560.200.200.160; C16.320.565.176.160; C16.320.565.189.168; C18.452.132.100.168; C18.452.648.176.160; C18.452.648.189.168; C18.452.845.500.075.160; C18.452.845.500.100.160
Unique ID: D028243
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D028243
Scope Note: A familial disorder marked by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES.
Entry Version: CEREBRAL AMYLOID ANGIOPATHY FAMILIAL
Entry Term(s): Amyloidosis VI; Amyloidosis, Cerebroarterial, Icelandic Type; Autosomal Dominant Cerebrovascular Amyloidosis; Cerebral Amyloid Angiopathy, Cst3-Related; Cerebral Amyloid Angiopathy, Genetic; Cerebral Amyloid Angiopathy, Hereditary; Cerebral Hemorrhage, Hereditary, With Amyloidosis; Familial Cerebral Amyloid Angiopathy; HCHWA; Hereditary Cerebral Amyloid Angiopathy; Hereditary Cerebral Amyloid Angiopathy, Icelandic Type; Hereditary Cerebral Hemorrhage With Amyloidosis; Icelandic Type Amyloidosis; Icelandic Type Hereditary Cerebral Amyloid Angiopathy
Previous Indexing: Amyloidosis (1974-1991); Cerebral Amyloid Angiopathy (1992-2001); Cerebrovascular Disorders (1974-1991)
Public MeSH Note: 2002; for CEREBRAL AMYLOID ANGIOPATHY, FAMILIAL see CEREBRAL AMYLOID ANGIOPATHY 2000-2001
History Note: 2002; for CEREBRAL AMYLOID ANGIOPATHY, FAMILIAL use CEREBRAL AMYLOID ANGIOPATHY 2000-2001
Date Established: 2002/01/01
Date of Entry: 2001/07/25
Revision Date: 2017/06/20

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
  - Brain Diseases [C10.228.140]
    - Brain Diseases, Metabolic [C10.228.140.163]
      - Brain Diseases, Metabolic, Inborn [C10.228.140.163.100]
        
        Adrenoleukodystrophy [C10.228.140.163.100.084]
        
        Cerebral Amyloid Angiopathy, Familial [C10.228.140.163.100.168]
        
        Galactosemias [C10.228.140.163.100.320]
        
        Hartnup Disease [C10.228.140.163.100.355]
        
        Hepatolenticular Degeneration [C10.228.140.163.100.360]
        
        Hereditary Central Nervous System Demyelinating Diseases [C10.228.140.163.100.362]
        
        Homocystinuria [C10.228.140.163.100.365]
        
        Hyperglycinemia, Nonketotic [C10.228.140.163.100.375]
        
        Hyperlysinemias [C10.228.140.163.100.380]
        
        Leigh Disease [C10.228.140.163.100.412]
        
        Lesch-Nyhan Syndrome [C10.228.140.163.100.425]
        
        Lysosomal Storage Diseases, Nervous System [C10.228.140.163.100.435]
        
        Maple Syrup Urine Disease [C10.228.140.163.100.520]
        
        MELAS Syndrome [C10.228.140.163.100.535]
        
        Menkes Kinky Hair Syndrome [C10.228.140.163.100.540]
        
        MERRF Syndrome [C10.228.140.163.100.545]
        
        Mevalonate Kinase Deficiency [C10.228.140.163.100.593]
        
        Oculocerebrorenal Syndrome [C10.228.140.163.100.640]
        
        Phenylketonurias [C10.228.140.163.100.687]
        
        Pyruvate Carboxylase Deficiency Disease [C10.228.140.163.100.725]
        
        Pyruvate Dehydrogenase Complex Deficiency Disease [C10.228.140.163.100.750]
        
        Refsum Disease [C10.228.140.163.100.813]
        
        Refsum Disease, Infantile [C10.228.140.163.100.844]
        
        Tyrosinemias [C10.228.140.163.100.875]
        
        Urea Cycle Disorders, Inborn [C10.228.140.163.100.937]
        
        Zellweger Syndrome [C10.228.140.163.100.968]

Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
  - Brain Diseases [C10.228.140]
    - Cerebrovascular Disorders [C10.228.140.300]
      - Cerebral Small Vessel Diseases [C10.228.140.300.275]
        
        CADASIL [C10.228.140.300.275.249]
        
        Cerebral Amyloid Angiopathy, Familial [C10.228.140.300.275.311]
        
        Fabry Disease [C10.228.140.300.275.374]
        
        MELAS Syndrome [C10.228.140.300.275.500]
        
        Microscopic Polyangiitis [C10.228.140.300.275.600]
        
        Stroke, Lacunar [C10.228.140.300.275.800]

Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
  - Brain Diseases [C10.228.140]
    - Cerebrovascular Disorders [C10.228.140.300]
      - Intracranial Arterial Diseases [C10.228.140.300.510]
        
        Cerebral Arterial Diseases [C10.228.140.300.510.200]
        
        Cerebral Amyloid Angiopathy [C10.228.140.300.510.200.200]
        
        Cerebral Amyloid Angiopathy, Familial [C10.228.140.300.510.200.200.160]

Cardiovascular Diseases [C14]
- Vascular Diseases [C14.907]
  - Cerebrovascular Disorders [C14.907.253]
    - Cerebral Small Vessel Diseases [C14.907.253.329]

Cardiovascular Diseases [C14]
- Vascular Diseases [C14.907]
  - Cerebrovascular Disorders [C14.907.253]
    - Intracranial Arterial Diseases [C14.907.253.560]
      - Cerebral Arterial Diseases [C14.907.253.560.200]
        
        Cerebral Amyloid Angiopathy [C14.907.253.560.200.200]
        
        Cerebral Amyloid Angiopathy, Familial [C14.907.253.560.200.200.160]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Metabolism, Inborn Errors [C16.320.565]
    - Amyloidosis, Familial [C16.320.565.176]
      - Amyloid Neuropathies, Familial [C16.320.565.176.050]
      - Cerebral Amyloid Angiopathy, Familial [C16.320.565.176.160]

Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
  - Metabolism, Inborn Errors [C16.320.565]
    - Brain Diseases, Metabolic, Inborn [C16.320.565.189]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Brain Diseases, Metabolic [C18.452.132]
    - Brain Diseases, Metabolic, Inborn [C18.452.132.100]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Metabolism, Inborn Errors [C18.452.648]
    - Amyloidosis, Familial [C18.452.648.176]
      - Amyloid Neuropathies, Familial [C18.452.648.176.050]
      - Cerebral Amyloid Angiopathy, Familial [C18.452.648.176.160]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Metabolism, Inborn Errors [C18.452.648]
    - Brain Diseases, Metabolic, Inborn [C18.452.648.189]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Proteostasis Deficiencies [C18.452.845]
    - Amyloidosis [C18.452.845.500]
      - Amyloidosis, Familial [C18.452.845.500.075]
        
        Amyloid Neuropathies, Familial [C18.452.845.500.075.050]
        
        Cerebral Amyloid Angiopathy, Familial [C18.452.845.500.075.160]

Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
  - Proteostasis Deficiencies [C18.452.845]
    - Amyloidosis [C18.452.845.500]
      - Cerebral Amyloid Angiopathy [C18.452.845.500.100]
        
        Cerebral Amyloid Angiopathy, Familial [C18.452.845.500.100.160]

Cerebral Amyloid Angiopathy, Familial Preferred

Hereditary Cerebral Amyloid Angiopathy, Icelandic Type Narrower

Cerebral Amyloid Angiopathy, Hereditary Narrower

Cerebral Amyloid Angiopathy, Genetic Narrower

Cerebral Amyloid Angiopathy, Familial MeSH Descriptor Data 2024