chromosome 1p36 deletion syndrome

Human disease
MedicalCondition developmental_defect_during_embryogenesis Q3297103
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chromosome 1p36 deletion syndrome

Summary

chromosome 1p36 deletion syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • chromosome 1p36 deletion syndrome's instance of is recorded as developmental defect during embryogenesis[3].
  • chromosome 1p36 deletion syndrome's instance of is recorded as designated intractable/rare disease[4].
  • chromosome 1p36 deletion syndrome's instance of is recorded as class of disease[5].
  • chromosome 1p36 deletion syndrome is a type of chromosomal deletion syndrome[6].
  • chromosome 1p36 deletion syndrome is a type of chromosomal anomaly with epilepsy as a major feature[7].
  • chromosome 1p36 deletion syndrome is a type of syndrome associated with dilated cardiomyopathy[8].
  • chromosome 1p36 deletion syndrome is a type of partial deletion of the short arm of chromosome 1[9].
  • chromosome 1p36 deletion syndrome is a type of disease[10].
  • chromosome 1p36 deletion syndrome's Commons category is recorded as 1p36 deletion syndrome[11].
  • chromosome 1p36 deletion syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4495[12].
  • chromosome 1p36 deletion syndrome's ICD-9-CM is recorded as 758.39[13].
  • chromosome 1p36 deletion syndrome's NCI Thesaurus ID is recorded as C74983[14].
  • chromosome 1p36 deletion syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060410[15].
  • chromosome 1p36 deletion syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060410[16].
  • chromosome 1p36 deletion syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1606[17].
  • chromosome 1p36 deletion syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].

Why It Matters

chromosome 1p36 deletion syndrome has Wikipedia articles in 13 language editions, a strong signal of global cultural recognition.[2] It is known by 14 alternative names across languages and contexts.[19]

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] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . Disease Ontology. Retrieved . wikidata.org.
  5. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . 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] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . ddrare.nibiohn.go.jp. Retrieved . ddrare.nibiohn.go.jp. Provenance: wikidata.org.
  11. [13] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] . Disease Ontology. Retrieved . wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [19] . 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). chromosome 1p36 deletion syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/chromosome-1p36-deletion-syndrome
MLA “chromosome 1p36 deletion syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/chromosome-1p36-deletion-syndrome.
BibTeX @misc{4ortxyz_chromosome-1p36-deletion-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{chromosome 1p36 deletion syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/chromosome-1p36-deletion-syndrome}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): chromosome 1p36 deletion syndrome — https://4ort.xyz/entity/chromosome-1p36-deletion-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/chromosome-1p36-deletion-syndrome · 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. 4h ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of
    Instance of developmental defect during embryogenesis, designated intractable/rare disease, class of disease
    Instance of
    Aliases
    + 2 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"
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