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progeroid syndrome

range of genetic disorders which cause a person to appear to grow older faster
Class type of: genetic disease, developmental defect during embryogenesis Q6139748

Facts

3 properties
Instance of
class of disease
Subclass of
genetic disease, developmental defect during embryogenesis[2][3]
Symptoms and signs
senescence, Prematurely aged appearance[4][5]
🏷️ Also known as
en progeroid syndrome en PS ar متلازمات شبيهة الشياخ es síndrome progeroide fa سندرم‌های پروجروید fr syndrome progéroïde ja 遅老 ja 早老症 ko 조로증 ru прогероидный синдром tr progeroid sendrom uk Прогероїдні синдроми zh 提早老化 zh 早老性症候群 zh 过早衰老
🔖 Identifiers · 16
OpenAlex ID
C2909947164
BabelNet ID
14105761n
Exact match
www.orpha.net
Freebase ID
/m/0dpvyc
ICD-11 ID (Foundation)
1520135105
ICD-11 ID (MMS)
LD2B
JSTOR topic ID (archived)
premature-aging
KBpedia ID
ProgeroidSyndrome
MeSH descriptor ID
D019588
MeSH tree code
C23.888.069
Microsoft Academic ID (discontinued)
2778113432
Mondo ID
MONDO_0015333
Show all 16 identifiers +4
NDL Authority ID
01120054
Orphanet ID
139033, 363245
Topic's main category
Category:Progeroid syndromes
UMLS CUI
C0231341, C5680983
📚 Sources · 1
  • ndl_authorities as of 2026-10-01 · 1 statement · pdl-1.0 data obtained from Web NDL Authorities (National Diet Library)

Report an error or request removal Lineage (PROV-JSON)

⛏️ Lake Facts · open-dataset statements via 4ort-mint

From open datasets, joined by identifier and shown only for properties Wikidata does not state on this entity — except where the dataset is the registry authority for the fact (ClinicalTrials.gov on trial registration data): there its value is shown instead, with Wikidata's noted beside it. Every row carries its dataset edition and licence.

Library of Congress Authorities IDP244
sh85107291 2026-10-01 ndl_authorities (pdl-1.0) as of 2026-10-01
where from?
Source
ndl_authorities
Edition
20261001 · as of 2026-10-01 · newer edition 20261103 landed
Licence
pdl-1.0
Credit
data obtained from Web NDL Authorities (National Diet Library)
Bronze
manifest sha256 6e048898660f1188…
Transform
4ort-mint · lake · version not recorded
data obtained from Web NDL Authorities (National Diet Library)
🔗 Connections
Subtypes 6
progeria, Werner syndrome, Rothmund-Thomson syndrome, Wiedemann-Rautenstrauch syndrome, Acrogeria, Barraquer–Simons syndrome
Subclass of 1
genetic disease
Symptoms and signs 1
senescence
Topic's main category 1
Category:Progeroid syndromes
← Category's main topic 1
Category:Progeroid syndromes
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Summary

progeroid syndrome is a class of disease[1].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). progeroid syndrome. Retrieved November 11, 2026, from https://4ort.xyz/entity/progeroid-syndrome
MLA “progeroid syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 11 Nov. 2026, https://4ort.xyz/entity/progeroid-syndrome.
BibTeX @misc{4ortxyz_progeroid-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{progeroid syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/progeroid-syndrome}, note = {Accessed: 2026-11-11}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): progeroid syndrome — https://4ort.xyz/entity/progeroid-syndrome (retrieved 2026-11-11)

Canonical URL: https://4ort.xyz/entity/progeroid-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. 16w ago · KrBot bot · 2026-07-23 view diff on Wikidata ↗
    Subclass of → genetic disease, developmental defect during embryogenesis
    "Removed claim: Subclass of: developmental defect during embryogenesis, дублирующееся значение / duplicate value"
  2. 18w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → genetic disease, developmental defect during embryogenesis
    Instance of → class of disease
    Topic's main category → Category:Progeroid syndromes
    Symptoms and signs → senescence, Prematurely aged appearance
    "Changed the item: QuickStatements 3.0 batch #39742: subclass of disease, not instance"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.