congenital stationary night blindness 1B

congenital stationary night blindness characterized by autosomal recessive inheritance that has material basis in mutation in the GRM6 gene on chromosome 5q35

Class type of: congenital stationary night blindness, genetic disease, autosomal recessive disease Q32144020

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Summary

congenital stationary night blindness 1B is a rare disease^[1]. It is a type of congenital stationary night blindness^[2], genetic disease^[3], and autosomal recessive disease^[4].

Key Facts

Instance of: class of disease^[5]
Genetic association: GRM6^[6]
On focus list of Wikimedia project: WikiProject Medicine^[7]

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Quick Facts

Instance of rare disease, class of disease

Subclass of congenital stationary night blindness, genetic disease, autosomal recessive disease

Properties

Genetic association GRM6

On focus list of wikimedia project WikiProject Medicine

Identifiers (6)

Disease ontology id DOID:0110865

Exact match purl.obolibrary.org, identifiers.org

Mondo id MONDO_0009758

Omim id 257270

Umls cui C1850362

Uniprot disease id DI-00377

🏷️ Also known as

en autosomal recessive complete congenital stationary night blindness en congenital stationary night blindness 1B en congenital stationary night blindness 1B autosomal recessive en congenital stationary night blindness type 1B en CSNB1B en Csnb, Complete, Autosomal Recessive en Night Blindness, Congenital Stationary, Complete, Autosomal Recessive en NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B en NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B; CSNB1B

References

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

Direct Wikidata claims

[5] ↑ congenital stationary night blindness 1B — instance of (P31): class of disease. wikidata.org.
[2] ↑ congenital stationary night blindness 1B — subclass of (P279): congenital stationary night blindness. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[3] ↑ congenital stationary night blindness 1B — subclass of (P279): genetic disease. Disease Ontology. Retrieved 2019-05-15. wikidata.org.
[4] ↑ congenital stationary night blindness 1B — subclass of (P279): autosomal recessive disease. Disease Ontology. Retrieved 2020-11-30. wikidata.org.
[6] ↑ congenital stationary night blindness 1B — genetic association (P2293): GRM6. UniProt. Retrieved 2019-08-13. wikidata.org.
[7] ↑ congenital stationary night blindness 1B — on focus list of Wikimedia project (P5008): WikiProject Medicine. wikidata.org.

Class ancestry

[1] ↑ congenital stationary night blindness 1B is an instance of rare disease (Q929833) [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). congenital stationary night blindness 1B. Retrieved October 30, 2026, from https://4ort.xyz/entity/congenital-stationary-night-blindness-1b

MLA

“congenital stationary night blindness 1B.” 4ort.xyz Knowledge Graph, 4ort.xyz, 30 Oct. 2026, https://4ort.xyz/entity/congenital-stationary-night-blindness-1b.

BibTeX

@misc{4ortxyz_congenital-stationary-night-blindness-1b_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{congenital stationary night blindness 1B}}, year = {2026}, url = {https://4ort.xyz/entity/congenital-stationary-night-blindness-1b}, note = {Accessed: 2026-10-30}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): congenital stationary night blindness 1B — https://4ort.xyz/entity/congenital-stationary-night-blindness-1b (retrieved 2026-10-30)

Canonical URL: https://4ort.xyz/entity/congenital-stationary-night-blindness-1b · Last refreshed: October 30, 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.

17w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗

Mondo id → MONDO_0009758

Imported from → —

Umls cui → C1850362

Disease ontology id → DOID:0110865

+ 8 other properties edited (see Wikidata diff for full list)

"/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39943|batch #39943]]: deprecate redundant disease superclasses"

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