hereditary elliptocytosis

hematopoietic system disease characterized by oval or elliptical red blood cells, slight or absent hemolysis with little or no anemia; splenomegaly is often present
MedicalCondition rare_disease Q2298020
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hereditary elliptocytosis

Summary

hereditary elliptocytosis is a rare disease[1]. It draws 162 Wikipedia views per month (rare_disease category, ranking #207 of 627).[2]

Key Facts

  • hereditary elliptocytosis's instance of is recorded as rare disease[3].
  • hereditary elliptocytosis's instance of is recorded as class of disease[4].
  • hereditary elliptocytosis is a type of hematopoietic system disease[5].
  • hereditary elliptocytosis is a type of disease[6].
  • hereditary elliptocytosis's Commons category is recorded as Hereditary elliptocytosis[7].
  • hereditary elliptocytosis's symptoms and signs is recorded as Elliptocyte[8].
  • hereditary elliptocytosis's ICD-9-CM is recorded as 282.1[9].
  • hereditary elliptocytosis's NCI Thesaurus ID is recorded as C35882[10].
  • hereditary elliptocytosis's health specialty is recorded as hematology[11].
  • hereditary elliptocytosis's genetic association is recorded as EPB41[12].
  • hereditary elliptocytosis's genetic association is recorded as SPTA1[13].
  • hereditary elliptocytosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2373[14].
  • hereditary elliptocytosis's exact match is recorded as http://identifiers.org/doid/DOID:2373[15].
  • hereditary elliptocytosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_288[16].
  • hereditary elliptocytosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].

Why It Matters

hereditary elliptocytosis draws 162 Wikipedia views per month (rare_disease category, ranking #207 of 627).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[18] It is known by 6 alternative names across languages and contexts.[19]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Disease Ontology. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . Disease Ontology. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Molecular basis of hereditary elliptocytosis due to protein 4.1 deficiency. wikidata.org.
  11. [13] . Mutant forms of spectrin alpha-subunits in hereditary elliptocytosis. wikidata.org.
  12. [14] . Disease Ontology. Retrieved . wikidata.org.
  13. [15] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [18] . Wikidata sitelinks. wikidata.org.
  3. [19] . Wikidata aliases. 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). hereditary elliptocytosis. Retrieved May 3, 2026, from https://4ort.xyz/entity/hereditary-elliptocytosis
MLA “hereditary elliptocytosis.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hereditary-elliptocytosis.
BibTeX @misc{4ortxyz_hereditary-elliptocytosis_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hereditary elliptocytosis}}, year = {2026}, url = {https://4ort.xyz/entity/hereditary-elliptocytosis}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hereditary elliptocytosis — https://4ort.xyz/entity/hereditary-elliptocytosis (retrieved 2026-05-03)

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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. 17d ago · Nyuhn · 2026-07-10 view diff on Wikidata ↗
    P14541 2tUi51
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/40849|batch #40849]]: ZGBK ID"
  2. 24d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of hematopoietic system disease, disease
    On focus list of wikimedia project WikiProject Medicine
    Health specialty hematology
    Genetic association EPB41, SPTA1
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.