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5D00.20 Hereditary ATTR amyloidosis

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

postcoordination

synonyms

• Hereditary ATTR amyloidosis
• familial neuropathic amyloidosis
• familial polyneuropathic amyloidosis
• AF type amyloidosis
• Neuropathic heredofamilial amyloidosis
• Transthyretin-related amyloidosis
• Familial amyloid polyneuropathy
• Portuguese amyloidosis
• Corino de Andrade paramyloidosis
• FAP - [familial amyloid polyneuropathy]
• Andrade type amyloid polyneuropathy
• Andrade syndrome
• familial amyloid neuropathy, Andrade type
• familial amyloid neuropathy, Portuguese type
• hereditary amyloid polyneuropathy Portuguese type
• hereditary neuropathic amyloidosis Type 1
• Japanese type amyloid polyneuropathy
• amyloid polyneuropathy type 1
• amyloid polyneuropathy
• amyloidosis Type 1
• polyneuropathy in amyloidosis
• Portuguese amyloid polyneuropathy
• Portuguese polyneuritic amyloidosis
• Portuguese type familial amyloid neuropathy
• Swiss type amyloid polyneuropathy
• Swedish type amyloid polyneuropathy
• type I familial amyloid polyneuropathy
• Wohlwill-Corino Andrade syndrome
• type II familial amyloid polyneuropathy
• Paramyloidosis
• familial amyloid polyneuropathy, 30 met-for-val
• Portuguese type amyloid polyneuropathy
• Cerebral neuropathic heredofamilial amyloidosis angiopathy
• Glomerular disorders in neuropathic heredofamilial amyloidosis
• Transthyretin-related familial amyloid cardiomyopathy
• Cardiac neuropathic heredofamilial amyloidosis
• ATTRV30M amyloidosis
• ATTRV122I amyloidosis

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