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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