multiple pterygium syndrome

Human disease
MedicalCondition genetic_disease Q16889762
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multiple pterygium syndrome

Summary

multiple pterygium syndrome is a genetic disease[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • multiple pterygium syndrome's instance of is recorded as genetic disease[3].
  • multiple pterygium syndrome's instance of is recorded as developmental defect during embryogenesis[4].
  • multiple pterygium syndrome's instance of is recorded as syndromic pterygium[5].
  • multiple pterygium syndrome's instance of is recorded as rare disease[6].
  • multiple pterygium syndrome's instance of is recorded as class of disease[7].
  • multiple pterygium syndrome is a type of autosomal recessive disease[8].
  • multiple pterygium syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[9].
  • multiple pterygium syndrome is a type of syndrome[10].
  • multiple pterygium syndrome is a type of genetic disease[11].
  • multiple pterygium syndrome is a type of monogenic disease[12].
  • multiple pterygium syndrome is a type of disease[13].
  • multiple pterygium syndrome's symptoms and signs is recorded as pterygium[14].
  • multiple pterygium syndrome's ICD-9-CM is recorded as 759.89[15].
  • multiple pterygium syndrome's NCI Thesaurus ID is recorded as C101039[16].
  • multiple pterygium syndrome's health specialty is recorded as dermatology[17].
  • multiple pterygium syndrome's genetic association is recorded as CHRNG[18].
  • multiple pterygium syndrome's genetic association is recorded as MYH3[19].
  • multiple pterygium syndrome's genetic association is recorded as CHRND[20].
  • multiple pterygium syndrome's genetic association is recorded as CHRNA1[21].
  • multiple pterygium syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080110[22].
  • multiple pterygium syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080110[23].
  • multiple pterygium syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2990[24].
  • multiple pterygium syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[25].

Why It Matters

multiple pterygium syndrome has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 18 alternative names across languages and contexts.[26]

References

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

Direct Wikidata claims

  1. [3] . 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] . Disease Ontology. Retrieved . wikidata.org.
  9. [11] . Disease Ontology. Retrieved . wikidata.org.
  10. [12] . Disease Ontology. Retrieved . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  14. [16] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  17. [19] . Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3.. wikidata.org.
  18. [20] . Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. wikidata.org.
  19. [21] . Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. wikidata.org.
  20. [22] . Disease Ontology. Retrieved . wikidata.org.
  21. [23] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [26] . 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). multiple pterygium syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/multiple-pterygium-syndrome
MLA “multiple pterygium syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/multiple-pterygium-syndrome.
BibTeX @misc{4ortxyz_multiple-pterygium-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{multiple pterygium syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/multiple-pterygium-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): multiple pterygium syndrome — https://4ort.xyz/entity/multiple-pterygium-syndrome (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. 24d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Instance of genetic disease, developmental defect during embryogenesis, syndromic pterygium +2
    Subclass of autosomal recessive disease, multiple congenital anomalies/dysmorphic syndrome without intellectual disability, syndrome +3
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
  2. 24d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Health specialty dermatology
    Genetic association CHRNG, MYH3, CHRND +1
    Subclass of
    Instance of genetic disease, developmental defect during embryogenesis, syndromic pterygium +2
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39732|batch #39732]]: rm redundant subclass"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.