Alves syndrome

human disease

MedicalCondition hereditary_disorder Q448838

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Alves syndrome

Summary

Alves syndrome is a hereditary disorder^[1].

Key Facts

Alves syndrome's instance of is recorded as hereditary disorder^[2].
Alves syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
Alves syndrome's instance of is recorded as class of disease^[4].
Alves syndrome is a type of neurogenic arthrogryposis multiplex congenita^[5].
Alves syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3354^[6].

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Quick Facts

Instance of class of disease

Subclass of neurogenic arthrogryposis multiplex congenita, developmental defect during embryogenesis, hereditary disorder

Properties

Exact match www.orpha.net

External References (8)

Gard rare disease id 1553

Google knowledge graph id /g/122mqfjr

Icd-11 id (foundation) 1206025469

Mesh descriptor id C536593

Mondo id MONDO_0011131

Omim id 601701

Orphanet id 3354

Umls cui C1866427, C2931256

References

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

Direct Wikidata claims

[2] ↑ Alves syndrome — instance of (P31): hereditary disorder. wikidata.org.
[3] ↑ Alves syndrome — instance of (P31): developmental defect during embryogenesis. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[4] ↑ Alves syndrome — instance of (P31): class of disease. wikidata.org.
[5] ↑ Alves syndrome — subclass of (P279): neurogenic arthrogryposis multiplex congenita. wikidata.org.
[6] ↑ Alves syndrome — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_3354. wikidata.org.

Class ancestry

[1] ↑ Alves syndrome 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). Alves syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/alves-syndrome

MLA “Alves syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/alves-syndrome.

BibTeX

@misc{4ortxyz_alves-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Alves syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/alves-syndrome}, note = {Accessed: 2026-05-03}}

LLM prompt

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

Canonical URL: https://4ort.xyz/entity/alves-syndrome · 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.

2d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0011131

Gard rare disease id → 1553

Orphanet id → 3354

Google knowledge graph id → /g/122mqfjr

+ 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"

Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.