Curry-Jones syndrome

medical condition
MedicalCondition developmental_defect_during_embryogenesis Q55783221
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Curry-Jones syndrome

Summary

Curry-Jones syndrome is a developmental defect during embryogenesis[1].

Key Facts

  • Curry-Jones syndrome's instance of is recorded as developmental defect during embryogenesis[2].
  • Curry-Jones syndrome's instance of is recorded as class of disease[3].
  • Curry-Jones syndrome is a type of genetic nervous system disorder[4].
  • Curry-Jones syndrome is a type of syndrome with corpus callosum agenesis /dysgenesis as a major feature[5].
  • Curry-Jones syndrome is a type of syndromic craniosynostosis[6].
  • Curry-Jones syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome[7].
  • Curry-Jones syndrome's genetic association is recorded as SMO[8].
  • Curry-Jones syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1553[9].

References

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

Direct Wikidata claims

  1. [2] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [5] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [6] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [8] . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  8. [9] . wikidata.org.

Class ancestry

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

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APA 4ort.xyz Knowledge Graph. (2026). Curry-Jones syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/curry-jones-syndrome
MLA “Curry-Jones syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/curry-jones-syndrome.
BibTeX @misc{4ortxyz_curry-jones-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Curry-Jones syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/curry-jones-syndrome}, note = {Accessed: 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. 26d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Mondo id MONDO_0011134
    Genetic association SMO
    Gard rare disease id 5584
    Orphanet id 1553
    + 9 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39742|batch #39742]]: subclass of disease, not instance"
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