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Meier-Gorlin syndrome 6

human disease
MedicalCondition developmental_defect_during_embryogenesis Q55785015
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Meier-Gorlin syndrome 6

Summary

Meier-Gorlin syndrome 6 is a developmental defect during embryogenesis[1]. It is known by 3 alternative names across languages and contexts.[2]

Key Facts

  • Meier-Gorlin syndrome 6's instance of is recorded as developmental defect during embryogenesis[3].
  • Meier-Gorlin syndrome 6's instance of is recorded as rare disease[4].
  • Meier-Gorlin syndrome 6's instance of is recorded as disease[5].
  • Meier-Gorlin syndrome 6's instance of is recorded as class of disease[6].
  • Meier-Gorlin syndrome 6 is a type of Meier-Gorlin syndrome[7].
  • Meier-Gorlin syndrome 6 is a type of autosomal dominant disease[8].
  • Meier-Gorlin syndrome 6's genetic association is recorded as GMNN[9].
  • Meier-Gorlin syndrome 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080517[10].
  • Meier-Gorlin syndrome 6's exact match is recorded as http://identifiers.org/doid/DOID:0080517[11].
  • Meier-Gorlin syndrome 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].

Why It Matters

Meier-Gorlin syndrome 6 is known by 3 alternative names across languages and contexts.[2]

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] ↑ . wikidata.org.
  3. [5] ↑ . Meier-Gorlin syndrome: report of eight additional cases and review.. wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [8] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [9] ↑ . Q905695. Retrieved . wikidata.org.
  8. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  9. [11] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  10. [12] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). Meier-Gorlin syndrome 6. Retrieved May 3, 2026, from https://4ort.xyz/entity/meier-gorlin-syndrome-6
MLA “Meier-Gorlin syndrome 6.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/meier-gorlin-syndrome-6.
BibTeX @misc{4ortxyz_meier-gorlin-syndrome-6_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Meier-Gorlin syndrome 6}}, year = {2026}, url = {https://4ort.xyz/entity/meier-gorlin-syndrome-6}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Meier-Gorlin syndrome 6 — https://4ort.xyz/entity/meier-gorlin-syndrome-6 (retrieved 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. 11w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id → MONDO_0014794
    Genetic association → GMNN
    Instance of → developmental defect during embryogenesis, rare disease, disease +1
    Imported from → —
    + 8 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39731|batch #39731]]: rm redundant P31"
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