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Primary systemic amyloidosis

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ORPHA:314701

Classification level: Subtype of disorder

Synonym(s):
  • Systemic AL amyloidosis

Prevalence: 1-5 / 10 000

Inheritance: Not applicable

Age of onset:

ICD-10: E85.0 , E85.1 , E85.2 , E85.3

OMIM: 254500

UMLS: C0281479

Summary

This disease is described under AL amyloidosis

Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

General public
Article for general public
Guidelines
Emergency guidelines
Français (2015.pdf) - Orphanet Urgences
Español (2017.pdf) - Orphanet Urgences
Disease review articles
Review article
Deutsch (2022) - Onkopedia
English (2024) - Ann Neurol
English (2012) - Orphanet J Rare Dis
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