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5D00.20 Hereditary ATTR amyloidosis
International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01
postcoordination
Add Stem and/or Extension codes to form a cluster code which adds detail to the condition.
Specific anatomy - multiple selections are allowed
Has manifestation - multiple selections are allowed
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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