RIN2 syndrome

MedicalCondition developmental_defect_during_embryogenesis Q55783958

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RIN2 syndrome

Summary

RIN2 syndrome is a developmental defect during embryogenesis^[1].

Key Facts

RIN2 syndrome's instance of is recorded as developmental defect during embryogenesis^[2].
RIN2 syndrome's instance of is recorded as rare disease^[3].
RIN2 syndrome's instance of is recorded as class of disease^[4].
RIN2 syndrome is a type of disease^[5].
RIN2 syndrome's genetic association is recorded as RIN2^[6].
RIN2 syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_217335^[7].

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Quick Facts

Instance of developmental defect during embryogenesis, rare disease, class of disease

Subclass of disease

Properties

Exact match www.orpha.net

Genetic association RIN2

External References (9)

Icd-10-cm Q82.8

Icd-11 id (foundation) 648412341

Kegg id H00906

Mesh descriptor id C567770

Mondo id MONDO_0013115

Omim id 613075

Orphanet id 217335

Umls cui C2751321

Uniprot disease id DI-02637

References

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

Direct Wikidata claims

[2] ↑ RIN2 syndrome — instance of (P31): developmental defect during embryogenesis. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[3] ↑ RIN2 syndrome — instance of (P31): rare disease. wikidata.org.
[4] ↑ RIN2 syndrome — instance of (P31): class of disease. wikidata.org.
[5] ↑ RIN2 syndrome — subclass of (P279): disease. wikidata.org.
[6] ↑ RIN2 syndrome — genetic association (P2293): RIN2. Q905695. Retrieved 2019-08-13. wikidata.org.
[7] ↑ RIN2 syndrome — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_217335. wikidata.org.

Class ancestry

[1] ↑ RIN2 syndrome is an instance of developmental defect during embryogenesis (Q55788864) [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). RIN2 syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/rin2-syndrome

MLA “RIN2 syndrome.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rin2-syndrome.

BibTeX

@misc{4ortxyz_rin2-syndrome_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{RIN2 syndrome}}, year = {2026}, url = {https://4ort.xyz/entity/rin2-syndrome}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): RIN2 syndrome — https://4ort.xyz/entity/rin2-syndrome (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/rin2-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.

6w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0013115

Genetic association → RIN2

Kegg id → H00906

Orphanet id → 217335

+ 9 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"

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