Cerebral Amyloid Angiopathy, Familial D028243

Related MeSH Hierarchy (12)

Diseases [C] » Cardiovascular Diseases [C14] » Vascular Diseases » Cerebrovascular Disorders » Cerebral Small Vessel Diseases » Cerebral Amyloid Angiopathy, Familial

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Brain Diseases, Metabolic » Brain Diseases, Metabolic, Inborn » Cerebral Amyloid Angiopathy, Familial

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Amyloidosis, Familial » Cerebral Amyloid Angiopathy, Familial

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Brain Diseases, Metabolic, Inborn » Cerebral Amyloid Angiopathy, Familial

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Proteostasis Deficiencies » Amyloidosis » Amyloidosis, Familial » Cerebral Amyloid Angiopathy, Familial

Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Proteostasis Deficiencies » Amyloidosis » Cerebral Amyloid Angiopathy » Cerebral Amyloid Angiopathy, Familial

Description

A familial disorder marked by AMYLOID deposits in the walls of small and medium sized blood vessels of CEREBRAL CORTEX and MENINGES.   MeSH

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Organization Involved with Phase 3 Indications (1)

Organization Involved with Other Experimental Indications (1)

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