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paraganglioma

human disease
MedicalCondition rare_disease Q581592
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paraganglioma

Summary

paraganglioma is a rare disease[1]. paraganglioma has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • paraganglioma's instance of is recorded as rare disease[3].
  • paraganglioma's instance of is recorded as class of disease[4].
  • paraganglioma is a type of phaeochromocytoma[5].
  • paraganglioma is a type of autosomal dominant disease[6].
  • paraganglioma's Commons category is recorded as Paraganglioma[7].
  • paraganglioma's ICD-9-CM is recorded as 239.7[8].
  • paraganglioma's NCI Thesaurus ID is recorded as C3308[9].
  • paraganglioma's health specialty is recorded as oncology[10].
  • paraganglioma's genetic association is recorded as SDHC[11].
  • paraganglioma's genetic association is recorded as SDHA[12].
  • paraganglioma's genetic association is recorded as SDHD[13].
  • paraganglioma's genetic association is recorded as SDHB[14].
  • paraganglioma's genetic association is recorded as SDHAF2[15].
  • paraganglioma's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050773[16].
  • paraganglioma's exact match is recorded as http://identifiers.org/doid/DOID:0050773[17].
  • paraganglioma's exact match is recorded as http://purl.obolibrary.org/obo/HP_0002668[18].
  • paraganglioma's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].

Why It Matters

paraganglioma has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2] paraganglioma is known by 13 alternative names across languages and contexts.[20]

Related Entities

oncology

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] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . Mutations in SDHC cause autosomal dominant paraganglioma, type 3.. wikidata.org.
  10. [12] ↑ . SDHA is a tumor suppressor gene causing paraganglioma. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  11. [13] ↑ . Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. wikidata.org.
  12. [14] ↑ . Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  13. [15] ↑ . SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma. wikidata.org.
  14. [16] ↑ . Disease Ontology. Retrieved . wikidata.org.
  15. [17] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  16. [18] ↑ . Human Phenotype Ontology release 2018-03-08. Retrieved . wikidata.org.
  17. [19] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. wikidata.org.
  2. [20] ↑ . 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). paraganglioma. Retrieved May 3, 2026, from https://4ort.xyz/entity/paraganglioma
MLA “paraganglioma.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/paraganglioma.
BibTeX @misc{4ortxyz_paraganglioma_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{paraganglioma}}, year = {2026}, url = {https://4ort.xyz/entity/paraganglioma}, note = {Accessed: 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. 7d ago · Nyuhn · 2026-07-10 view diff on Wikidata ↗
    P14541 → 368VMD
    Instance of → rare disease, class of disease
    On focus list of wikimedia project → WikiProject Medicine
    Subclass of → phaeochromocytoma, autosomal dominant disease
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/40849|batch #40849]]: ZGBK ID"
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