OMOP Concept 4260823

Familial amyloid polyneuropathy, type II

StandardConditionSNOMED4463009Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

3 source codes normalize to Familial amyloid polyneuropathy, type II via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Familial amyloid polyneuropathy, type II across source vocabularies.

  • amiloidosis neuropática hereditaria, tipo II
  • amiloidosis, tipo Indiana - Maryland
  • Amyloidosis, Indiana-Maryland type
  • Familial amyloid polyneuropathy, 84 Ser-for-Ile
  • Familial amyloid polyneuropathy, Indiana-Swiss type
  • Familial amyloid polyneuropathy type II
  • Familial amyloid polyneuropathy, type II (disorder)
  • German type amyloid polyneuropathy
  • Hereditary neuropathic amyloidosis, type II
  • Indiana-Maryland type amyloid polyneuropathy
  • polineuropatía amiloide familiar, 84 Ser - for - Ile
  • polineuropatía amiloide familiar, tipo II
  • polineuropatía amiloide familiar, tipo II (trastorno)
  • polineuropatía amiloide familiar, tipo indiana suiza
  • Rakavina type amyloidosis
  • Swiss type amyloid polyneuropathy

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

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