Aldolase A deficiency

medical condition
MedicalCondition rare_disease Q4713937
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Aldolase A deficiency

Summary

Aldolase A deficiency is a rare disease[1]. It draws 36 Wikipedia views per month (rare_disease category, ranking #234 of 627).[2]

Key Facts

  • Aldolase A deficiency's instance of is recorded as rare disease[3].
  • Aldolase A deficiency's instance of is recorded as class of disease[4].
  • Aldolase A deficiency is a type of hemolytic anemia[5].
  • Aldolase A deficiency is a type of glycogen storage disease[6].
  • Aldolase A deficiency is a type of disorder of glycolysis[7].
  • Aldolase A deficiency is a type of hemolytic anemia due to a disorder of glycolytic enzymes[8].
  • Aldolase A deficiency's Commons category is recorded as Aldolase A deficiency[9].
  • Aldolase A deficiency's ICD-9-CM is recorded as 282.3[10].
  • Aldolase A deficiency's health specialty is recorded as endocrinology[11].
  • Aldolase A deficiency's genetic association is recorded as ALDOA[12].
  • Aldolase A deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_57[13].

Why It Matters

Aldolase A deficiency draws 36 Wikipedia views per month (rare_disease category, ranking #234 of 627).[2]

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] . 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] . wikidata.org.
  8. [10] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Human aldolase A deficiency associated with a hemolytic anemia: thermolabile aldolase due to a single base mutation. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  11. [13] . wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). Aldolase A deficiency. Retrieved May 3, 2026, from https://4ort.xyz/entity/aldolase-a-deficiency
MLA “Aldolase A deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/aldolase-a-deficiency.
BibTeX @misc{4ortxyz_aldolase-a-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Aldolase A deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/aldolase-a-deficiency}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Aldolase A deficiency — https://4ort.xyz/entity/aldolase-a-deficiency (retrieved 2026-05-03)

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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. 7w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Gard rare disease id 600
    Health specialty endocrinology
    Icd-9-cm 282.3
    Imported from
    + 18 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39953|batch #39953]]: deprecate redundant disease superclasses (2)"
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