5D00.20

ICD-11 MMS 2026-01

Hereditary ATTR amyloidosis

Index terms

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

Exclusions from above levels

  • 6D80 – Dementia due to Alzheimer disease
  • 2B31.2 – histiocytosis X (chronic)
  • 3A10.Z – Hereditary haemolytic anaemia due to enzyme deficiency
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  • 5A71.01 – Congenital adrenal hyperplasia
  • 5A81.1 – 5-alpha-reductase deficiency
  • LD28.01 – Marfan syndrome
  • LD28.1 – Ehlers-Danlos syndrome
  • LD2A.4 – androgen resistance syndrome
  • 18 – Pregnancy, childbirth or the puerperium
  • http://id.who.int/icd/entity/1004987305 – Transitory endocrine or metabolic disorders specific to fetus or newborn

Sibling codes

  • 5D00.21 – Non-neuropathic heredofamilial amyloidosis
  • 5D00.2Y – Other specified hereditary amyloidosis
  • 5D00.2Z – Hereditary amyloidosis, unspecified

Foundation entity

Hereditary ATTR amyloidosis – http://id.who.int/icd/entity/807065795

Allowed postcoordination axes

Part of: 5D00.2: Hereditary amyloidosis › 5D00: Amyloidosis › 05: Endocrine, nutritional or metabolic diseases