All
 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