Glycogen storage disease type XI

Fanconi-Bickel glycogenosis (FBG) is a rare glycogen storage disease characterized by hepatorenal glycogen accumulation, severe renal tubular dysfunction and impaired glucose and galactose metabolism
MedicalCondition rare_disease Q5572613
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Glycogen storage disease type XI

Summary

Glycogen storage disease type XI is a rare disease[1]. It draws 11 Wikipedia views per month (rare_disease category, ranking #230 of 627).[2]

Key Facts

  • Glycogen storage disease type XI's instance of is recorded as rare disease[3].
  • Glycogen storage disease type XI's instance of is recorded as class of disease[4].
  • Glycogen storage disease type XI's subclass of is recorded as glycogen storage disease[5].
  • Glycogen storage disease type XI's subclass of is recorded as glucose transport disorder[6].
  • Glycogen storage disease type XI's subclass of is recorded as nephropathy secondary to a storage or other metabolic disease[7].
  • Glycogen storage disease type XI's subclass of is recorded as rare metabolic liver disease[8].
  • Glycogen storage disease type XI's OMIM ID is recorded as 227810[9].
  • Glycogen storage disease type XI's DiseasesDB is recorded as 31709[10].
  • Glycogen storage disease type XI's KEGG ID is recorded as H01947[11].
  • Glycogen storage disease type XI's Encyclopædia Britannica Online ID is recorded as science/glycogenosis-type-XI[12].
  • Glycogen storage disease type XI's Orphanet ID is recorded as 2088[13].
  • Glycogen storage disease type XI's NCI Thesaurus ID is recorded as C168998[14].
  • Glycogen storage disease type XI's genetic association is recorded as SLC2A2[15].
  • Glycogen storage disease type XI's BabelNet ID is recorded as 00950709n[16].
  • Glycogen storage disease type XI's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2088[17].
  • Glycogen storage disease type XI's UMLS CUI is recorded as C3495427[18].
  • Glycogen storage disease type XI's ICD-10-CM is recorded as E74.0[19].
  • Glycogen storage disease type XI's GARD rare disease ID is recorded as 2268[20].
  • Glycogen storage disease type XI's Mondo ID is recorded as MONDO_0009216[21].
  • Glycogen storage disease type XI's Microsoft Academic ID is recorded as 2777037749[22].
  • Glycogen storage disease type XI's ICD-11 ID is recorded as 426701963[23].
  • Glycogen storage disease type XI's WikiProjectMed ID is recorded as Fanconi–Bickel syndrome[24].
  • Glycogen storage disease type XI's UniProt disease ID is recorded as DI-02478[25].

Why It Matters

Glycogen storage disease type XI draws 11 Wikipedia views per month (rare_disease category, ranking #230 of 627).[2] It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[26] It is known by 24 alternative names across languages and contexts.[27]

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] . wikidata.org.
  4. [6] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  7. [9] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [10] . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  14. [16] . BabelNet. wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  17. [19] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  18. [20] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [26] . Wikidata sitelinks. wikidata.org.
  3. [27] . 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). Glycogen storage disease type XI. Retrieved May 3, 2026, from https://4ort.xyz/entity/glycogen-storage-disease-type-xi
MLA “Glycogen storage disease type XI.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/glycogen-storage-disease-type-xi.
BibTeX @misc{4ortxyz_glycogen-storage-disease-type-xi_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Glycogen storage disease type XI}}, year = {2026}, url = {https://4ort.xyz/entity/glycogen-storage-disease-type-xi}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Glycogen storage disease type XI — https://4ort.xyz/entity/glycogen-storage-disease-type-xi (retrieved 2026-05-03)

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