BNAR syndrome

MedicalCondition head_and_neck_disease Q55783626

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BNAR syndrome

Summary

BNAR syndrome is a head and neck disease^[1].

Key Facts

BNAR syndrome's instance of is recorded as head and neck disease^[2].
BNAR syndrome's instance of is recorded as developmental defect during embryogenesis^[3].
BNAR syndrome's instance of is recorded as rare disease^[4].
BNAR syndrome's instance of is recorded as class of disease^[5].
BNAR syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability^[6].
BNAR syndrome is a type of syndromic anorectal malformation^[7].
BNAR syndrome is a type of syndromic renal or urinary tract malformation^[8].
BNAR syndrome is a type of Bifid nose^[9].
BNAR syndrome's genetic association is recorded as FREM1^[10].
BNAR syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_217266^[11].

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Quick Facts

Instance of rare disease, class of disease

Subclass of multiple congenital anomalies/dysmorphic syndrome without intellectual disability, syndromic anorectal malformation, syndromic renal or urinary tract malformation, Bifid nose, developmental defect during embryogenesis, head and neck disease

Properties

Exact match www.orpha.net

Genetic association FREM1

External References (9)

Gard rare disease id 10595

Icd-10-cm Q87.8

Kegg id H00685

Mesh descriptor id C567672

Mondo id MONDO_0012165

Omim id 608980

Orphanet id 217266

Umls cui C2750433

Uniprot disease id DI-02627

References

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

Direct Wikidata claims

[2] ↑ BNAR syndrome — instance of (P31): head and neck disease. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[3] ↑ BNAR syndrome — instance of (P31): developmental defect during embryogenesis. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[4] ↑ BNAR syndrome — instance of (P31): rare disease. wikidata.org.
[5] ↑ BNAR syndrome — instance of (P31): class of disease. wikidata.org.
[6] ↑ BNAR syndrome — subclass of (P279): multiple congenital anomalies/dysmorphic syndrome without intellectual disability. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[7] ↑ BNAR syndrome — subclass of (P279): syndromic anorectal malformation. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[8] ↑ BNAR syndrome — subclass of (P279): syndromic renal or urinary tract malformation. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[9] ↑ BNAR syndrome — subclass of (P279): Bifid nose. wikidata.org.
[10] ↑ BNAR syndrome — genetic association (P2293): FREM1. Q905695. Retrieved 2019-08-13. platform.opentargets.org. Provenance: wikidata.org.
[11] ↑ BNAR syndrome — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_217266. wikidata.org.

Class ancestry

[1] ↑ BNAR syndrome is an instance of head and neck disease (Q55789477) [P31, primary]. Wikidata. 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). BNAR syndrome. Retrieved May 3, 2026, from https://4ort.xyz/entity/bnar-syndrome

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

BibTeX

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

LLM prompt

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

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

7w ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗

Mondo id → MONDO_0012165

Genetic association → FREM1

Kegg id → H00685

Orphanet id → 217266

+ 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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