Cerebral Amyloid Angiopathy, Familial
"Cerebral Amyloid Angiopathy, Familial" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A familial disorder marked by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES.
Descriptor ID |
D028243
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MeSH 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
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Concept/Terms |
Hereditary Cerebral Amyloid Angiopathy, Icelandic Type- Hereditary Cerebral Amyloid Angiopathy, Icelandic Type
- 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
Cerebral Amyloid Angiopathy, Hereditary- Cerebral Amyloid Angiopathy, Hereditary
- Hereditary Cerebral Amyloid Angiopathy
- Hereditary Cerebral Hemorrhage With Amyloidosis
- Cerebral Hemorrhage, Hereditary, With Amyloidosis
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Below are MeSH descriptors whose meaning is more general than "Cerebral Amyloid Angiopathy, Familial".
- Diseases [C]
- 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]
- Cerebral Amyloid Angiopathy, Familial [C10.228.140.163.100.168]
- Cerebrovascular Disorders [C10.228.140.300]
- Cerebral Small Vessel Diseases [C10.228.140.300.275]
- Cerebral Amyloid Angiopathy, Familial [C10.228.140.300.275.311]
- 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]
- Cerebral Amyloid Angiopathy, Familial [C14.907.253.329.311]
- 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]
- Cerebral Amyloid Angiopathy, Familial [C16.320.565.176.160]
- Brain Diseases, Metabolic, Inborn [C16.320.565.189]
- Cerebral Amyloid Angiopathy, Familial [C16.320.565.189.168]
- Nutritional and Metabolic Diseases [C18]
- Metabolic Diseases [C18.452]
- Brain Diseases, Metabolic [C18.452.132]
- Brain Diseases, Metabolic, Inborn [C18.452.132.100]
- Cerebral Amyloid Angiopathy, Familial [C18.452.132.100.168]
- Metabolism, Inborn Errors [C18.452.648]
- Amyloidosis, Familial [C18.452.648.176]
- Cerebral Amyloid Angiopathy, Familial [C18.452.648.176.160]
- Brain Diseases, Metabolic, Inborn [C18.452.648.189]
- Cerebral Amyloid Angiopathy, Familial [C18.452.648.189.168]
- Proteostasis Deficiencies [C18.452.845]
- Amyloidosis [C18.452.845.500]
- Amyloidosis, Familial [C18.452.845.500.075]
- Cerebral Amyloid Angiopathy, Familial [C18.452.845.500.075.160]
- Cerebral Amyloid Angiopathy [C18.452.845.500.100]
- Cerebral Amyloid Angiopathy, Familial [C18.452.845.500.100.160]
Below are MeSH descriptors whose meaning is more specific than "Cerebral Amyloid Angiopathy, Familial".
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