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3-M syndrome

autosomal recessive disease characterized by dwarfism, facial dysmorphia and skeletal abnormalities
MedicalCondition rare_disease Q3335660
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3-M syndrome

Summary

3-M syndrome is a rare disease[1]. It draws 22 Wikipedia views per month (rare_disease category, ranking #216 of 627).[2]

Key Facts

  • 3-M syndrome's instance of is recorded as rare disease[3].
  • 3-M syndrome's instance of is recorded as class of disease[4].
  • 3-M syndrome's subclass of is recorded as autosomal recessive disease[5].
  • 3-M syndrome's subclass of is recorded as syndrome[6].
  • 3-M syndrome's MeSH descriptor ID is recorded as C535725[7].
  • 3-M syndrome's MeSH descriptor ID is recorded as C535314[8].
  • 3-M syndrome's OMIM ID is recorded as 273750[9].
  • 3-M syndrome's OMIM ID is recorded as 612921[10].
  • 3-M syndrome's OMIM ID is recorded as 614205[11].
  • 3-M syndrome's DiseasesDB is recorded as 33510[12].
  • 3-M syndrome's KEGG ID is recorded as H00509[13].
  • 3-M syndrome's GeneReviews ID is recorded as NBK1481[14].
  • 3-M syndrome's Disease Ontology ID is recorded as DOID:0060241[15].
  • 3-M syndrome's Orphanet ID is recorded as 2616[16].
  • 3-M syndrome's health specialty is recorded as medical genetics[17].
  • 3-M syndrome's genetic association is recorded as OBSL1[18].
  • 3-M syndrome's genetic association is recorded as CUL7[19].
  • 3-M syndrome's genetic association is recorded as CCDC8[20].
  • 3-M syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060241[21].
  • 3-M syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060241[22].
  • 3-M syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2616[23].
  • 3-M syndrome's UMLS CUI is recorded as C1848862[24].
  • 3-M syndrome's UMLS CUI is recorded as C1851996[25].
  • 3-M syndrome's Quora topic ID is recorded as 3-M-Syndrome[26].
  • 3-M syndrome's GARD rare disease ID is recorded as 5667[27].

Why It Matters

3-M syndrome draws 22 Wikipedia views per month (rare_disease category, ranking #216 of 627).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] It is known by 9 alternative names across languages and contexts.[29]

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] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [9] ↑ . Disease Ontology. Retrieved . wikidata.org.
  8. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [11] ↑ . Disease Ontology. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Disease Ontology. Retrieved . wikidata.org.
  14. [16] ↑ . Disease Ontology. Retrieved . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . The primordial growth disorder 3-M syndrome connects ubiquitination to the cytoskeletal adaptor OBSL1.. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  17. [19] ↑ . Identification of mutations in CUL7 in 3-M syndrome. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  18. [20] ↑ . Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  19. [21] ↑ . Disease Ontology. Retrieved . wikidata.org.
  20. [22] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . Disease Ontology. Retrieved . wikidata.org.
  23. [25] ↑ . Disease Ontology. Retrieved . wikidata.org.
  24. [26] ↑ . Quora. 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.

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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). 3-M syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/3-m-syndrome
MLA “3-M syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/3-m-syndrome.
BibTeX @misc{4ortxyz_3-m-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3-M syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/3-m-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 3-M syndrome — https://4ort.xyz/entity/3-m-syndrome (retrieved 2026-05-03)

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