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tritanomaly

Human disease
Class type of: anomalous trichromacy, tritanopia, congenital color blindness Q6152917

Facts

2 properties
Instance of
rare disease
Subclass of
anomalous trichromacy, tritanopia, congenital color blindness
🏷️ Also known as
en blue-yellow color blindness en blue–yellow color blindness en tritanomaly de Tritanomalie es tritanomalía ja 先天青黄異常 ja 3型3色覚 ja 第3色弱 ja 青色弱 pl tritanomalia ru неразличимость синего и жёлтого цветов ru тританомалия
🔖 Identifiers · 5
Brockhaus Enzyklopädie online ID
tritanomalie
Google Knowledge Graph ID
/g/11r7rlj7v
Human Phenotype Ontology ID
HP:0000552
IEV number
845-22-033
WikiSkripta article ID
51024

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🔗 Connections
Instance of 1
rare disease
Subclass of 1
tritanopia
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Summary

tritanomaly is a rare disease[1]. tritanomaly is a type of anomalous trichromacy[2], tritanopia[3], and congenital color blindness[4].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . 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). tritanomaly. Retrieved November 10, 2026, from https://4ort.xyz/entity/tritanomaly
MLA “tritanomaly.” 4ort.xyz Knowledge Graph, 4ort.xyz, 10 Nov. 2026, https://4ort.xyz/entity/tritanomaly.
BibTeX @misc{4ortxyz_tritanomaly_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{tritanomaly}}, year = {2026}, url = {https://4ort.xyz/entity/tritanomaly}, note = {Accessed: 2026-11-10}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): tritanomaly — https://4ort.xyz/entity/tritanomaly (retrieved 2026-11-10)

Canonical URL: https://4ort.xyz/entity/tritanomaly · Last refreshed:

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.

  1. 3d ago · VastV0idInSpace0 · 2026-11-09 view diff on Wikidata ↗
    Human Phenotype Ontology ID → HP:0000552
    Instance of → rare disease
    Subclass of → anomalous trichromacy, tritanopia, congenital color blindness
    "Created claim: Human Phenotype Ontology ID: HP:0000552, Matched to Tritanomaly (#19256013) in HPO #mix'n'match"
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