asplenia

congenital disorder
MedicalCondition rare_disease Q737712
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asplenia

Summary

asplenia is a rare disease[1]. asplenia draws 36 Wikipedia views per month (rare_disease category, ranking #209 of 627).[2]

Key Facts

  • asplenia's instance of is recorded as rare disease[3].
  • asplenia's instance of is recorded as disease[4].
  • asplenia's subclass of is recorded as splenic disease[5].
  • asplenia's subclass of is recorded as hyposplenism[6].
  • asplenia's OMIM ID is recorded as 208530[7].
  • asplenia's OMIM ID is recorded as 208540[8].
  • asplenia's ICD-9 ID is recorded as 289.59[9].
  • asplenia's ICD-9 ID is recorded as 759.01[10].
  • asplenia's ICD-10 ID is recorded as D73.0[11].
  • asplenia's ICD-10 ID is recorded as Q89.0[12].
  • asplenia's Freebase ID is recorded as /m/03txc3[13].
  • asplenia's eMedicine ID is recorded as 885226[14].
  • asplenia's eMedicine ID is recorded as 406116[15].
  • asplenia's Patientplus ID is recorded as splenectomy-hyposplenism-and-asplenia[16].
  • asplenia's different from is recorded as Asplenia[17].
  • asplenia's health specialty is recorded as medical genetics[18].
  • asplenia's genetic association is recorded as NPHP3[19].
  • asplenia's PatientsLikeMe condition ID is recorded as asplenia[20].
  • asplenia's SNOMED CT ID is recorded as 707147002[21].
  • asplenia's Microsoft Academic ID is recorded as 2779335628[22].
  • asplenia's Microsoft Academic ID is recorded as 2908974829[23].
  • asplenia's OpenAlex ID is recorded as C2779335628[24].

Why It Matters

asplenia draws 36 Wikipedia views per month (rare_disease category, ranking #209 of 627).[2] asplenia has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[25] asplenia is known by 5 alternative names across languages and contexts.[26]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . Congenital absence of the spleen; syndrome with atrioventricularis and situs inversus; case reports and review of the literature.. wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Freebase Data Dumps. wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . patient.co.uk. patient.co.uk. Provenance: wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia. wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . OpenAlex. Retrieved . docs.openalex.org. Provenance: wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [25] . Wikidata sitelinks. wikidata.org.
  3. [26] . 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). asplenia. Retrieved May 3, 2026, from https://4ort.xyz/entity/asplenia
MLA “asplenia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/asplenia.
BibTeX @misc{4ortxyz_asplenia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{asplenia}}, year = {2026}, url = {https://4ort.xyz/entity/asplenia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): asplenia — https://4ort.xyz/entity/asplenia (retrieved 2026-05-03)

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