Meier-Gorlin syndrome

autosomal recessive disorder characterized by severe intrauterine and postnatal growth retardation, microcephaly, bilateral microtia and hypoplastic patellae
MedicalCondition rare_disease Q19587381
Press Enter · cited answer in seconds

Meier-Gorlin syndrome

Summary

Meier-Gorlin syndrome is a rare disease[1]. It draws 5 Wikipedia views per month (rare_disease category, ranking #233 of 627).[2]

Key Facts

  • Meier-Gorlin syndrome's instance of is recorded as rare disease[3].
  • Meier-Gorlin syndrome's instance of is recorded as class of disease[4].
  • Meier-Gorlin syndrome's subclass of is recorded as syndrome[5].
  • Meier-Gorlin syndrome's MeSH descriptor ID is recorded as C538012[6].
  • Meier-Gorlin syndrome's KEGG ID is recorded as H01889[7].
  • Meier-Gorlin syndrome's Disease Ontology ID is recorded as DOID:0060306[8].
  • Meier-Gorlin syndrome's Orphanet ID is recorded as 2554[9].
  • Meier-Gorlin syndrome's ICD-9-CM is recorded as 759.89[10].
  • Meier-Gorlin syndrome's genetic association is recorded as ORC1[11].
  • Meier-Gorlin syndrome's genetic association is recorded as ORC6[12].
  • Meier-Gorlin syndrome's genetic association is recorded as CDC45[13].
  • Meier-Gorlin syndrome's genetic association is recorded as CDC6[14].
  • Meier-Gorlin syndrome's genetic association is recorded as ORC4[15].
  • Meier-Gorlin syndrome's genetic association is recorded as CDT1[16].
  • Meier-Gorlin syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060306[17].
  • Meier-Gorlin syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060306[18].
  • Meier-Gorlin syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2554[19].
  • Meier-Gorlin syndrome's UMLS CUI is recorded as CN030358[20].
  • Meier-Gorlin syndrome's UMLS CUI is recorded as C1868684[21].
  • Meier-Gorlin syndrome's GARD rare disease ID is recorded as 2033[22].
  • Meier-Gorlin syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[23].
  • Meier-Gorlin syndrome's Mondo ID is recorded as MONDO_0016817[24].

Why It Matters

Meier-Gorlin syndrome draws 5 Wikipedia views per month (rare_disease category, ranking #233 of 627).[2]

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] . wikidata.org.
  6. [8] . Disease Ontology. Retrieved . wikidata.org.
  7. [9] . Disease Ontology. Retrieved . wikidata.org.
  8. [10] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  10. [12] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  11. [13] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  12. [14] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  13. [15] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  14. [16] . Open Targets Platform. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  15. [17] . Disease Ontology. Retrieved . wikidata.org.
  16. [18] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  19. [21] . Disease Ontology. Retrieved . wikidata.org.
  20. [22] . Disease Ontology. Retrieved . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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. Retrieved May 3, 2026, from https://4ort.xyz/entity/meier-gorlin-syndrome
MLA “Meier-Gorlin syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/meier-gorlin-syndrome.
BibTeX @misc{4ortxyz_meier-gorlin-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Meier-Gorlin syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/meier-gorlin-syndrome}, 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 — https://4ort.xyz/entity/meier-gorlin-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/meier-gorlin-syndrome · Last refreshed: