properdin deficiency

human disease
MedicalCondition rare_disease Q7250189
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properdin deficiency

Summary

properdin deficiency is a rare disease[1]. It draws 1 Wikipedia views per month (rare_disease category, ranking #237 of 627).[2]

Key Facts

  • properdin deficiency's instance of is recorded as rare disease[3].
  • properdin deficiency's instance of is recorded as class of disease[4].
  • properdin deficiency's subclass of is recorded as complement deficiency[5].
  • properdin deficiency's subclass of is recorded as immunodeficiency due to a complement regulatory deficiency[6].
  • properdin deficiency's subclass of is recorded as X-linked recessive disease[7].
  • properdin deficiency's MeSH descriptor ID is recorded as C537241[8].
  • properdin deficiency's OMIM ID is recorded as 312060[9].
  • properdin deficiency's Disease Ontology ID is recorded as DOID:0111768[10].
  • properdin deficiency's Orphanet ID is recorded as 2966[11].
  • properdin deficiency's ICD-9-CM is recorded as 279.8[12].
  • properdin deficiency's genetic association is recorded as CFP[13].
  • properdin deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2966[14].
  • properdin deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111768[15].
  • properdin deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0111768[16].
  • properdin deficiency's UMLS CUI is recorded as C1839456[17].
  • properdin deficiency's UMLS CUI is recorded as C1839455[18].
  • properdin deficiency's UMLS CUI is recorded as C1839454[19].
  • properdin deficiency's UMLS CUI is recorded as C0398762[20].
  • properdin deficiency's ICD-10-CM is recorded as D84.1[21].
  • properdin deficiency's GARD rare disease ID is recorded as 4513[22].
  • properdin deficiency's Mondo ID is recorded as MONDO_0010713[23].
  • properdin deficiency's Microsoft Academic ID is recorded as 2910352300[24].
  • properdin deficiency's WikiProjectMed ID is recorded as Properdin deficiency[25].
  • properdin deficiency's UniProt disease ID is recorded as DI-02220[26].

Why It Matters

properdin deficiency draws 1 Wikipedia views per month (rare_disease category, ranking #237 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] . Disease Ontology. Retrieved . wikidata.org.
  4. [6] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  5. [7] . Disease Ontology. 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] . Disease Ontology. 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] . Sequence-based analysis of properdin deficiency: identification of point mutations in two phenotypic forms of an X-linked immunodeficiency. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Disease Ontology. Retrieved . wikidata.org.
  14. [16] . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  15. [17] . Monarch Disease Ontology release 2018-06-29. Retrieved . 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] . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . wikidata.org.
  24. [26] . 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). properdin deficiency. Retrieved May 3, 2026, from https://4ort.xyz/entity/properdin-deficiency
MLA “properdin deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/properdin-deficiency.
BibTeX @misc{4ortxyz_properdin-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{properdin deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/properdin-deficiency}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): properdin deficiency — https://4ort.xyz/entity/properdin-deficiency (retrieved 2026-05-03)

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