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3MC syndrome 1

3MC syndrome associated with the MASP1 gene on chromosome 3q27
MedicalCondition rare_disease Q6837320
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Summary

3MC syndrome 1 is a rare disease[1]. It draws 122 Wikipedia views per month (rare disease category, ranking #236 of 627).[2]

Key Facts

  • Instance of: class of disease[3]
  • Subclass of: 3MC syndrome[4]
  • Health specialty: medical genetics[5]
  • Genetic association: MASP1[6]
  • Exact match: http://purl.obolibrary.org/obo/DOID_0060575[7], http://identifiers.org/doid/DOID:0060575[8]
  • On focus list of Wikimedia project: WikiProject Medicine[9]
  • Has phenotype: Q141815887[10]
  • P14914: D02506[11]

Why It Matters

3MC syndrome 1 is known by 4 alternative names across languages and contexts.[12]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . MASP1 mutations in patients with facial, umbilical, coccygeal, and auditory findings of Carnevale, Malpuech, OSA, and Michels syndromes. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  5. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [8] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [12] ↑ . 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). 3MC syndrome 1. Retrieved October 28, 2026, from https://4ort.xyz/entity/3mc-syndrome-1
MLA “3MC syndrome 1.” 4ort.xyz Knowledge Graph, 4ort.xyz, 28 Oct. 2026, https://4ort.xyz/entity/3mc-syndrome-1.
BibTeX @misc{4ortxyz_3mc-syndrome-1_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3MC syndrome 1}}, year = {2026}, url = {https://4ort.xyz/entity/3mc-syndrome-1}, note = {Accessed: 2026-10-28}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 3MC syndrome 1 — https://4ort.xyz/entity/3mc-syndrome-1 (retrieved 2026-10-28)

Canonical URL: https://4ort.xyz/entity/3mc-syndrome-1 · Last refreshed:

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. 5d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Uniprot disease id → DI-03129
    Mondo id → MONDO_0009770
    Instance of → rare disease, class of disease
    Exact match → http://purl.obolibrary.org/obo/DOID_0060575, http://identifiers.org/doid/DOID:0060575
    + 16 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.