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AL amyloidosis

medical condition
Class type of: amyloidosis, plasma cell neoplasm, lymphoproliferative disorders Q4652470

Facts

8 properties
Instance of
designated intractable/rare disease, class of disease[2]
Subclass of
amyloidosis, plasma cell neoplasm, lymphoproliferative disorders, paraproteinemia[3][4][5][6]
Age of onset
adult onset[10]
Has phenotype
fatigue, kidney disease, nephrotic syndrome, congenital heart disease, hypertrophic cardiomyopathy, malabsorption, interstitial lung disease, hypergammaglobulinemia, Wikidata item, Wikidata item, kidney failure, xerostomia, elevated alkaline phosphatase, Wikidata item, salivary gland disease, peripheral edema, Wikidata item, Jaw claudication, dry cough, Howell–Jolly body, macroglossia, dysphonia, dysphagia, gastroparesis[11][12][13][14][15][16][17][18][19][20][21][22][23][24]
Health specialty
endocrinology[9]
NCI Thesaurus ID
C158963[8]
P14914
D85443[25]
Prevalence
+0.00005[7]
🏷️ Also known as
en Light-chain amyloidosis en Primary amyloidosis en Systemic amyloidosis en AL amyloidosis en immunoglobulin light-chain amyloidosis da AL Amyloidose da Amyloid Let-kæde amyloidose de AL-Amyloidose fr amylose AL fr amylose primitive it Amiloidosi AL ja 全身性ALアミロイドーシス sv AL-amyloidos zh 初級類澱粉症
🔖 Identifiers · 23
OpenAlex ID
C2779551797, C2780945303
BabelNet ID
01017975n
DiseasesDB
315
EMedicine ID
208839
Exact match
www.orpha.net
External data available at URL
www.nanbyou.or.jp
GARD rare disease ID
5797
ICD-10 ID
E85
ICD-10-CM
E85.9
ICD-11 ID (Foundation)
1061366491
ICD-11 ID (MMS)
5D00.0
ICD-9 ID
277.3
Show all 23 identifiers +11
ICD-O
9769/1
MeSH descriptor ID
D000075363
MeSH tree code
C04.557.595.250, C18.452.845.500.550, C20.683.515.507, C20.683.780.565
Medical Dictionary for Regulatory Activities ID
10002022
MedlinePlus ID
000533
Microsoft Academic ID (discontinued)
2.9B (2.8B–2.9B, n=3)
Mondo ID
MONDO_0019438
OMIM ID
254500
Orphanet ID
85443
UMLS CUI
C0268381
WikiProjectMed ID
AL amyloidosis

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🔗 Connections
Subclass of 3
amyloidosis, lymphoproliferative disorders, paraproteinemia
Health specialty 1
endocrinology
← Cause of death 1
Jill Singer
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Summary

AL amyloidosis is a designated intractable/rare disease[1].

Related Entities

endocrinology

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . Retrieved . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Retrieved . wikidata.org.
  10. [11] ↑ . Retrieved . wikidata.org.
  11. [12] ↑ . Retrieved . wikidata.org.
  12. [13] ↑ . Retrieved . wikidata.org.
  13. [14] ↑ . Retrieved . wikidata.org.
  14. [15] ↑ . Retrieved . wikidata.org.
  15. [16] ↑ . Retrieved . wikidata.org.
  16. [17] ↑ . Retrieved . wikidata.org.
  17. [18] ↑ . Retrieved . wikidata.org.
  18. [19] ↑ . Retrieved . wikidata.org.
  19. [20] ↑ . Retrieved . wikidata.org.
  20. [21] ↑ . Retrieved . wikidata.org.
  21. [22] ↑ . Retrieved . wikidata.org.
  22. [23] ↑ . Retrieved . wikidata.org.
  23. [24] ↑ . Retrieved . wikidata.org.
  24. [25] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). AL amyloidosis. Retrieved November 6, 2026, from https://4ort.xyz/entity/al-amyloidosis
MLA “AL amyloidosis.” 4ort.xyz Knowledge Graph, 4ort.xyz, 6 Nov. 2026, https://4ort.xyz/entity/al-amyloidosis.
BibTeX @misc{4ortxyz_al-amyloidosis_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{AL amyloidosis}}, year = {2026}, url = {https://4ort.xyz/entity/al-amyloidosis}, note = {Accessed: 2026-11-06}}
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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 16d ago · ACorrêa (WMB) · 2026-10-24 view diff on Wikidata ↗
    Prevalence → {'amount': '+0.00005'}
    Age of onset → adult onset
    Has phenotype → fatigue, kidney disease, nephrotic syndrome +21
    P14914 → D85443
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Health specialty → endocrinology
    Subclass of → amyloidosis, plasma cell neoplasm, lymphoproliferative disorders +1
    Instance of → designated intractable/rare disease, class of disease
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39953|batch #39953]]: deprecate redundant disease superclasses (2)"
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