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C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 + C16.320 Genetic Diseases, Inborn D030342 + C16.320.565 Metabolism, Inborn Errors D008661 + C16.320.565.100 Amyloidosis, Familial D028226 + C16.320.565.100.050 Amyloid Neuropathies, Familial D028227 C16.320.565.100.160 Cerebral Amyloid Angiopathy, Familial D028243
C18 Nutritional and Metabolic Diseases D009750 + C18.452 Metabolic Diseases D008659 + C18.452.090 Amyloidosis D000686 + C18.452.090.075 Amyloidosis, Familial D028226 + C18.452.090.075.050 Amyloid Neuropathies, Familial D028227 C18.452.090.075.160 Cerebral Amyloid Angiopathy, Familial D028243
C18 Nutritional and Metabolic Diseases D009750 + C18.452 Metabolic Diseases D008659 + C18.452.648 Metabolism, Inborn Errors D008661 + C18.452.648.100 Amyloidosis, Familial D028226 + C18.452.648.100.050 Amyloid Neuropathies, Familial D028227 C18.452.648.100.160 Cerebral Amyloid Angiopathy, Familial D028243