galactosemia

carbohydrate metabolic disorder that involves a defect in galactose metabolism resulting in toxic levels of galactose 1-phosphate in various tissues
MedicalCondition rare_disease Q774483
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galactosemia

Summary

galactosemia is a rare disease[1]. galactosemia draws 72 Wikipedia views per month (rare_disease category, ranking #106 of 627).[2]

Key Facts

  • galactosemia's instance of is recorded as rare disease[3].
  • galactosemia's instance of is recorded as class of disease[4].
  • galactosemia is a type of carbohydrate metabolic disorder[5].
  • galactosemia is a type of disorder of galactose metabolism[6].
  • galactosemia is a type of disease[7].
  • galactosemia's Commons category is recorded as Galactosemia[8].
  • galactosemia's symptoms and signs is recorded as lactose intolerance[9].
  • galactosemia's ICD-9-CM is recorded as 271.1[10].
  • galactosemia's NCI Thesaurus ID is recorded as C84723[11].
  • galactosemia's health specialty is recorded as endocrinology[12].
  • galactosemia's genetic association is recorded as GALT[13].
  • galactosemia's genetic association is recorded as GALE[14].
  • galactosemia's exact match is recorded as http://purl.obolibrary.org/obo/DOID_9870[15].
  • galactosemia's exact match is recorded as http://identifiers.org/doid/DOID:9870[16].
  • galactosemia's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].

Why It Matters

galactosemia draws 72 Wikipedia views per month (rare_disease category, ranking #106 of 627).[2] galactosemia has Wikipedia articles in 19 language editions, a strong signal of global cultural recognition.[18] galactosemia is known by 3 alternative names across languages and contexts.[19]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Disease Ontology. Retrieved . wikidata.org.
  4. [6] . wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . Disease Ontology. Retrieved . wikidata.org.
  9. [11] . Disease Ontology. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Interallelic Complementation in Hybrid Cells Derived from Human Diploid Strains Deficient in Galactose-1-Phosphate Uridyl Transferase Activity. wikidata.org.
  12. [14] . Molecular characterization of a unique patient with epimerase‐deficiency galactosaemia. wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  15. [17] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [18] . Wikidata sitelinks. wikidata.org.
  3. [19] . Wikidata aliases. 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). galactosemia. Retrieved May 3, 2026, from https://4ort.xyz/entity/galactosemia
MLA “galactosemia.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/galactosemia.
BibTeX @misc{4ortxyz_galactosemia_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{galactosemia}}, year = {2026}, url = {https://4ort.xyz/entity/galactosemia}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): galactosemia — https://4ort.xyz/entity/galactosemia (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/galactosemia · 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. 7d ago · Twofivesixbot bot · 2026-05-26 view diff on Wikidata ↗
    Health specialty endocrinology
    Symptoms and signs lactose intolerance
    Instance of rare disease, class of disease
    Subclass of
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbsetclaim-update-qualifiers:1||1|4 */ [[Property:P8189]]: 987012431025705171, mv to monolingual text names on J9U statements"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.