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Myeloperoxidase deficiency

human disease
MedicalCondition rare_disease Q6947340
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Myeloperoxidase deficiency

Summary

Myeloperoxidase deficiency is a rare disease[1]. It draws 54 Wikipedia views per month (rare_disease category, ranking #234 of 627).[2]

Key Facts

  • Myeloperoxidase deficiency's instance of is recorded as rare disease[3].
  • Myeloperoxidase deficiency's instance of is recorded as class of disease[4].
  • Myeloperoxidase deficiency is a type of immune disorder[5].
  • Myeloperoxidase deficiency is a type of functional neutrophil defect[6].
  • Myeloperoxidase deficiency's ICD-9-CM is recorded as 288.8[7].
  • Myeloperoxidase deficiency's genetic association is recorded as MPO[8].
  • Myeloperoxidase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2587[9].

Why It Matters

Myeloperoxidase deficiency draws 54 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] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  6. [8] ↑ . Aberrant restriction endonuclease digests of DNA from subjects with hereditary myeloperoxidase deficiency.. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  7. [9] ↑ . 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). Myeloperoxidase deficiency. Retrieved May 3, 2026, from https://4ort.xyz/entity/myeloperoxidase-deficiency
MLA “Myeloperoxidase deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/myeloperoxidase-deficiency.
BibTeX @misc{4ortxyz_myeloperoxidase-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Myeloperoxidase deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/myeloperoxidase-deficiency}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Myeloperoxidase deficiency — https://4ort.xyz/entity/myeloperoxidase-deficiency (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/myeloperoxidase-deficiency · 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. 23d ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Emedicine id → 887599
    Gard rare disease id → 3868
    Icd-9-cm → 288.8
    Imported from → —
    + 16 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)"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.