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Catel–Manzke syndrome

Catel-Manzke syndrome is a rare bone disease characterized by bilateral hyperphalangy and clinodactyly of the index finger typically in association with Pierre Robin sequence (see this term) comprising micrognathia, cleft palate and glossoptosis
MedicalCondition head_and_neck_disease Q5051865
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Catel–Manzke syndrome

Summary

Catel–Manzke syndrome is a head and neck disease[1]. It draws 7 Wikipedia views per month (head_and_neck_disease category, ranking #54 of 92).[2]

Key Facts

  • Catel–Manzke syndrome's instance of is recorded as head and neck disease[3].
  • Catel–Manzke syndrome's instance of is recorded as developmental defect during embryogenesis[4].
  • Catel–Manzke syndrome's instance of is recorded as rare disease[5].
  • Catel–Manzke syndrome's instance of is recorded as class of disease[6].
  • Catel–Manzke syndrome's subclass of is recorded as Pierre Robin syndrome[7].
  • Catel–Manzke syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8].
  • Catel–Manzke syndrome's subclass of is recorded as orofacial clefting syndrome[9].
  • Catel–Manzke syndrome's subclass of is recorded as genetic syndromic intellectual disability[10].
  • Catel–Manzke syndrome's subclass of is recorded as syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy[11].
  • Catel–Manzke syndrome's MeSH descriptor ID is recorded as C535347[12].
  • Catel–Manzke syndrome's OMIM ID is recorded as 302380[13].
  • Catel–Manzke syndrome's OMIM ID is recorded as 616145[14].
  • Catel–Manzke syndrome's DiseasesDB is recorded as 33832[15].
  • Catel–Manzke syndrome's KEGG ID is recorded as H01845[16].
  • Catel–Manzke syndrome's Orphanet ID is recorded as 1388[17].
  • Catel–Manzke syndrome's genetic association is recorded as TGDS[18].
  • Catel–Manzke syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1388[19].
  • Catel–Manzke syndrome's UMLS CUI is recorded as C1844887[20].
  • Catel–Manzke syndrome's ICD-10-CM is recorded as Q87.8[21].
  • Catel–Manzke syndrome's GARD rare disease ID is recorded as 28[22].
  • Catel–Manzke syndrome's Mondo ID is recorded as MONDO_0014507[23].
  • Catel–Manzke syndrome's Microsoft Academic ID is recorded as 2778984006[24].
  • Catel–Manzke syndrome's ICD-11 ID is recorded as 1023183031[25].
  • Catel–Manzke syndrome's UniProt disease ID is recorded as DI-04301[26].

Why It Matters

Catel–Manzke syndrome draws 7 Wikipedia views per month (head_and_neck_disease category, ranking #54 of 92).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[27] It is known by 14 alternative names across languages and contexts.[28]

References

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

Direct Wikidata claims

  1. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [13] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  16. [18] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  17. [19] ↑ . wikidata.org.
  18. [20] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  19. [21] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  20. [22] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [27] ↑ . Wikidata sitelinks. wikidata.org.
  3. [28] ↑ . Wikidata aliases. 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). Catel–Manzke syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/catel-manzke-syndrome
MLA “Catel–Manzke syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/catel-manzke-syndrome.
BibTeX @misc{4ortxyz_catel-manzke-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Catel–Manzke syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/catel-manzke-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Catel–Manzke syndrome — https://4ort.xyz/entity/catel-manzke-syndrome (retrieved 2026-05-03)

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