hereditary cryohydrocytosis with normal stomatin

human disease
MedicalCondition rare_disease Q55781516
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hereditary cryohydrocytosis with normal stomatin

Summary

hereditary cryohydrocytosis with normal stomatin is a rare disease[1].

Key Facts

  • hereditary cryohydrocytosis with normal stomatin's instance of is recorded as rare disease[2].
  • hereditary cryohydrocytosis with normal stomatin's instance of is recorded as class of disease[3].
  • hereditary cryohydrocytosis with normal stomatin's subclass of is recorded as hereditary stomatocytosis[4].
  • hereditary cryohydrocytosis with normal stomatin's MeSH descriptor ID is recorded as C535827[5].
  • hereditary cryohydrocytosis with normal stomatin's OMIM ID is recorded as 185020[6].
  • hereditary cryohydrocytosis with normal stomatin's KEGG ID is recorded as H02002[7].
  • hereditary cryohydrocytosis with normal stomatin's Orphanet ID is recorded as 398088[8].
  • hereditary cryohydrocytosis with normal stomatin's genetic association is recorded as SLC4A1[9].
  • hereditary cryohydrocytosis with normal stomatin's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_398088[10].
  • hereditary cryohydrocytosis with normal stomatin's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_90044[11].
  • hereditary cryohydrocytosis with normal stomatin's UMLS CUI is recorded as C1861453[12].
  • hereditary cryohydrocytosis with normal stomatin's ICD-10-CM is recorded as D58.8[13].
  • hereditary cryohydrocytosis with normal stomatin's GARD rare disease ID is recorded as 10184[14].
  • hereditary cryohydrocytosis with normal stomatin's Mondo ID is recorded as MONDO_0008494[15].
  • hereditary cryohydrocytosis with normal stomatin's ICD-11 ID is recorded as 1764091350[16].

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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] . Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  9. [10] . wikidata.org.
  10. [11] . wikidata.org.
  11. [12] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [13] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.

Class ancestry

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

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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 cryohydrocytosis with normal stomatin. Retrieved May 3, 2026, from https://4ort.xyz/entity/hereditary-cryohydrocytosis-with-normal-stomatin
MLA “hereditary cryohydrocytosis with normal stomatin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hereditary-cryohydrocytosis-with-normal-stomatin.
BibTeX @misc{4ortxyz_hereditary-cryohydrocytosis-with-normal-stomatin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hereditary cryohydrocytosis with normal stomatin}}, year = {2026}, url = {https://4ort.xyz/entity/hereditary-cryohydrocytosis-with-normal-stomatin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hereditary cryohydrocytosis with normal stomatin — https://4ort.xyz/entity/hereditary-cryohydrocytosis-with-normal-stomatin (retrieved 2026-05-03)

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