Home › Entities › developmental_defect_during_embryogenesis › alpha-mannosidosis

alpha-mannosidosis

lysosomal storage disease that has material basis in deficiency of the alpha-D-manosidase enzyme resulting in the impairment of cell function from a build up of complex sugars derived from glycoproteins in the lysosome
MedicalCondition developmental_defect_during_embryogenesis Q250449
Press Enter · cited answer in seconds

alpha-mannosidosis

Summary

alpha-mannosidosis is a developmental defect during embryogenesis[1]. alpha-mannosidosis has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • alpha-mannosidosis's instance of is recorded as developmental defect during embryogenesis[3].
  • alpha-mannosidosis's instance of is recorded as rare disease[4].
  • alpha-mannosidosis's instance of is recorded as class of disease[5].
  • alpha-mannosidosis is a type of lysosomal storage disease[6].
  • alpha-mannosidosis is a type of Mannosidosis[7].
  • alpha-mannosidosis is a type of neurometabolic disease[8].
  • alpha-mannosidosis is a type of oligosaccharidosis[9].
  • alpha-mannosidosis is a type of rare genetic developmental defect during embryogenesis[10].
  • alpha-mannosidosis is a type of lysosomal storage disease with skeletal involvement[11].
  • alpha-mannosidosis is a type of metabolic disease with cataract[12].
  • alpha-mannosidosis is a type of metabolic disease with corneal opacity[13].
  • alpha-mannosidosis is a type of cataract associated with a metabolic disease[14].
  • alpha-mannosidosis's Commons category is recorded as Alpha-mannosidosis[15].
  • alpha-mannosidosis's ICD-9-CM is recorded as 271.8[16].
  • alpha-mannosidosis's NCI Thesaurus ID is recorded as C84548[17].
  • alpha-mannosidosis's health specialty is recorded as endocrinology[18].
  • alpha-mannosidosis's genetic association is recorded as MAN2B1[19].
  • alpha-mannosidosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3413[20].
  • alpha-mannosidosis's exact match is recorded as http://identifiers.org/doid/DOID:3413[21].
  • alpha-mannosidosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_61[22].
  • alpha-mannosidosis's on focus list of Wikimedia project is recorded as WikiProject Medicine[23].

Why It Matters

alpha-mannosidosis has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] alpha-mannosidosis is known by 12 alternative names across languages and contexts.[24]

Related Entities

endocrinology

References

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

Direct Wikidata claims

  1. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . wikidata.org.
  4. [6] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [7] ↑ . 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] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  10. [12] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  11. [13] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  12. [14] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  13. [15] ↑ . wikidata.org.
  14. [16] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  15. [17] ↑ . Disease Ontology. Retrieved . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . Q905695. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  18. [20] ↑ . Disease Ontology. Retrieved . wikidata.org.
  19. [21] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. wikidata.org.
  2. [24] ↑ . 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). alpha-mannosidosis. Retrieved May 3, 2026, from https://4ort.xyz/entity/alpha-mannosidosis
MLA “alpha-mannosidosis.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/alpha-mannosidosis.
BibTeX @misc{4ortxyz_alpha-mannosidosis_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{alpha-mannosidosis}}, year = {2026}, url = {https://4ort.xyz/entity/alpha-mannosidosis}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): alpha-mannosidosis — https://4ort.xyz/entity/alpha-mannosidosis (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/alpha-mannosidosis · 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. 17d ago · JhealdBatch bot · 2026-07-03 view diff on Wikidata ↗
    Subclass of → lysosomal storage disease, Mannosidosis, neurometabolic disease +6
    Health specialty → endocrinology
    Genetic association → MAN2B1
    Subclass of → —
    + 4 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"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.