Acrocephalopolydactyly

MedicalCondition hereditary_disorder Q17122137

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Acrocephalopolydactyly

Summary

Acrocephalopolydactyly is a hereditary disorder^[1].

Key Facts

Acrocephalopolydactyly's instance of is recorded as hereditary disorder^[2].
Acrocephalopolydactyly's instance of is recorded as developmental defect during embryogenesis^[3].
Acrocephalopolydactyly's instance of is recorded as class of disease^[4].
Acrocephalopolydactyly is a type of syndromic craniosynostosis^[5].
Acrocephalopolydactyly's different from is recorded as Griscelli syndrome type 1^[6].
Acrocephalopolydactyly's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_221054^[7].

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Quick Facts

Instance of class of disease

Subclass of syndromic craniosynostosis, developmental defect during embryogenesis, hereditary disorder

Properties

Different from Griscelli syndrome type 1

Exact match www.orpha.net

External References (9)

Gard rare disease id 2096

Google knowledge graph id /g/11bbmk2fsr

Icd-10-cm Q87.0

Mesh descriptor id C573722

Mondo id MONDO_0008709

Omim id 200995

Orphanet id 221054

Umls cui C3495588, C1860157

Uniprot disease id DI-01519

References

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

Direct Wikidata claims

[2] ↑ Acrocephalopolydactyly — instance of (P31): hereditary disorder. wikidata.org.
[3] ↑ Acrocephalopolydactyly — instance of (P31): developmental defect during embryogenesis. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[4] ↑ Acrocephalopolydactyly — instance of (P31): class of disease. wikidata.org.
[5] ↑ Acrocephalopolydactyly — subclass of (P279): syndromic craniosynostosis. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[6] ↑ Acrocephalopolydactyly — different from (P1889): Griscelli syndrome type 1. omim.org. omim.org. Provenance: wikidata.org.
[7] ↑ Acrocephalopolydactyly — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_221054. wikidata.org.

Class ancestry

[1] ↑ Acrocephalopolydactyly is an instance of hereditary disorder (Q3311537) [P31, primary]. 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). Acrocephalopolydactyly. Retrieved May 3, 2026, from https://4ort.xyz/entity/acrocephalopolydactyly

MLA

“Acrocephalopolydactyly.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/acrocephalopolydactyly.

BibTeX

@misc{4ortxyz_acrocephalopolydactyly_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Acrocephalopolydactyly}}, year = {2026}, url = {https://4ort.xyz/entity/acrocephalopolydactyly}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Acrocephalopolydactyly — https://4ort.xyz/entity/acrocephalopolydactyly (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/acrocephalopolydactyly · Last refreshed: May 3, 2026

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.

24d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0008709

Gard rare disease id → 2096

Orphanet id → 221054

Google knowledge graph id → /g/11bbmk2fsr

+ 10 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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