Begreppsinformation
...
Central Nervous System Diseases
Brain Diseases
Cerebrovascular Disorders
Cerebral Small Vessel Diseases
...
Cerebrovascular Disorders
Intracranial Arterial Diseases
Cerebral Arterial Diseases
Cerebral Amyloid Angiopathy
...
Cerebrovascular Disorders
Intracranial Arterial Diseases
Cerebral Arterial Diseases
Cerebral Amyloid Angiopathy
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Amyloidosis, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Amyloidosis, Familial
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Brain Diseases, Metabolic, Inborn
Föredragen term
Cerebral Amyloid Angiopathy, Familial
Typ
-
Topical Descriptor
Överordnat begrepp
Hänvisningstermer
- Autosomal Dominant Cerebrovascular Amyloidosis
- Familial Cerebral Amyloid Angiopathy
- HCHWA
Användningsanmärkning
- A familial disorder marked by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES.
Anmärkning om ändringshistoria
- 2002; for CEREBRAL AMYLOID ANGIOPATHY, FAMILIAL use CEREBRAL AMYLOID ANGIOPATHY 2000-2001
Termer på andra språk
-
finska
-
familiaalinen aivojen amyloidiangiopatia
-
familiaarinen aivojen amyloidiangiopatia
-
svenska
URI
http://www.yso.fi/onto/mesh/D028243
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