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uniparental disomy

presence in a cell of two paired chromosomes from the same parent, with no chromosome of that pair from the other parent
Class type of: chromosome abnormality Q1207929

Facts

1 property
Subclass of
chromosome abnormality
🏷️ Also known as
en uniparental disomy en UPD ar تكرار أحادي الأبوين de Heterodisomie de Isodisomie de Uniparentale Disomie es Disomía uniparental es Disomia uniparental fr disomie uniparentale he UPD he דיזומיה חד הורית he דיסומיה חד הורית hu egyszülős diszómia it disomia uniparentale ja 片親性ダイソミー ko 단친성 이염색체 ko 단친 이염색체성 pl Disomia jednorodzicielska pl heterodisomia pl izodisomia
🔖 Identifiers · 12
OpenAlex ID
C2780332060
Encyclopædia Britannica Online ID
topic/uniparental-disomy
Freebase ID
/m/01_0g4
Gran Enciclopèdia Catalana ID
disomia-uniparental
Gran Enciclopèdia Catalana ID (former scheme)
0271245
Human Phenotype Ontology ID
HP:0032382
ICD-10 ID
Q99.8
ICD-11 ID (Foundation)
694223526
ICD-11 ID (MMS)
LD45
MeSH descriptor ID
D024182
MeSH tree code
C23.550.210.645.890, G05.365.590.175.935
Microsoft Academic ID (discontinued)
2780332060

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🔗 Connections
Subclass of 1
chromosome abnormality
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Summary

uniparental disomy is a type of chromosome abnormality[1].

References

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

Direct Wikidata claims

  1. [1] ↑ . wikidata.org.

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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). uniparental disomy. Retrieved November 3, 2026, from https://4ort.xyz/entity/uniparental-disomy
MLA “uniparental disomy.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 Nov. 2026, https://4ort.xyz/entity/uniparental-disomy.
BibTeX @misc{4ortxyz_uniparental-disomy_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{uniparental disomy}}, year = {2026}, url = {https://4ort.xyz/entity/uniparental-disomy}, note = {Accessed: 2026-11-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): uniparental disomy — https://4ort.xyz/entity/uniparental-disomy (retrieved 2026-11-03)

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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. 13d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Wikipedia languages → ['ar', 'bs', 'ca', 'de', 'en', 'es', 'fr', 'gl', 'he', 'it', 'ja', 'ko', 'pl', '
    Subclass of → —
    Subclass of → chromosome abnormality
    Human Phenotype Ontology ID → HP:0032382
    + 1 other property edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61242|batch #61242]]: HPO ID through mesh or umls"
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