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congenital central hypoventilation syndrome

Human disease
MedicalCondition rare_disease Q979129
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congenital central hypoventilation syndrome

Summary

congenital central hypoventilation syndrome is a rare disease[1]. It draws 138 Wikipedia views per month (rare_disease category, ranking #126 of 627).[2]

Key Facts

  • congenital central hypoventilation syndrome's instance of is recorded as rare disease[3].
  • congenital central hypoventilation syndrome's instance of is recorded as class of disease[4].
  • congenital central hypoventilation syndrome's subclass of is recorded as autonomic nervous system disease[5].
  • congenital central hypoventilation syndrome's subclass of is recorded as genetic disease[6].
  • congenital central hypoventilation syndrome's subclass of is recorded as autosomal dominant disease[7].
  • congenital central hypoventilation syndrome's subclass of is recorded as disease[8].
  • congenital central hypoventilation syndrome's Commons category is recorded as Central hypoventilation syndrome[9].
  • congenital central hypoventilation syndrome's MeSH descriptor ID is recorded as C536209[10].
  • congenital central hypoventilation syndrome's OMIM ID is recorded as 209880[11].
  • congenital central hypoventilation syndrome's ICD-9 ID is recorded as 348.8[12].
  • congenital central hypoventilation syndrome's DiseasesDB is recorded as 32976[13].
  • congenital central hypoventilation syndrome's MedlinePlus ID is recorded as 000078[14].
  • congenital central hypoventilation syndrome's Freebase ID is recorded as /m/03cmv8[15].
  • congenital central hypoventilation syndrome's KEGG ID is recorded as H00916[16].
  • congenital central hypoventilation syndrome's GeneReviews ID is recorded as NBK1427[17].
  • congenital central hypoventilation syndrome's eMedicine ID is recorded as 1002927[18].
  • congenital central hypoventilation syndrome's Disease Ontology ID is recorded as DOID:0060731[19].
  • congenital central hypoventilation syndrome's Orphanet ID is recorded as 661[20].
  • congenital central hypoventilation syndrome's Orphanet ID is recorded as 99803[21].
  • congenital central hypoventilation syndrome's NCI Thesaurus ID is recorded as C98889[22].
  • congenital central hypoventilation syndrome's health specialty is recorded as neurology[23].
  • congenital central hypoventilation syndrome's genetic association is recorded as GDNF[24].
  • congenital central hypoventilation syndrome's genetic association is recorded as PHOX2B[25].
  • congenital central hypoventilation syndrome's genetic association is recorded as ASCL1[26].
  • congenital central hypoventilation syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060731[27].

Why It Matters

congenital central hypoventilation syndrome draws 138 Wikipedia views per month (rare_disease category, ranking #126 of 627).[2] It has Wikipedia articles in 17 language editions, a strong signal of global cultural recognition.[28] It is known by 39 alternative names across languages and contexts.[29]

Related Entities

disease neurology

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] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [8] ↑ . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . Disease Ontology. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Freebase Data Dumps. wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . Disease Ontology. Retrieved . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. wikidata.org.
  23. [25] ↑ . Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  24. [26] ↑ . Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse). wikidata.org.
  25. [27] ↑ . Disease Ontology. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . Wikidata sitelinks. wikidata.org.
  3. [29] ↑ . 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). congenital central hypoventilation syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/congenital-central-hypoventilation-syndrome
MLA “congenital central hypoventilation syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/congenital-central-hypoventilation-syndrome.
BibTeX @misc{4ortxyz_congenital-central-hypoventilation-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{congenital central hypoventilation syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/congenital-central-hypoventilation-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): congenital central hypoventilation syndrome — https://4ort.xyz/entity/congenital-central-hypoventilation-syndrome (retrieved 2026-05-03)

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