primary CD59 deficiency

human disease

MedicalCondition rare_disease Q55783887

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primary CD59 deficiency

Summary

primary CD59 deficiency is a rare disease^[1].

Key Facts

primary CD59 deficiency's instance of is recorded as rare disease^[2].
primary CD59 deficiency's instance of is recorded as class of disease^[3].
primary CD59 deficiency's subclass of is recorded as immunodeficiency due to a complement regulatory deficiency^[4].
primary CD59 deficiency's subclass of is recorded as genetic peripheral neuropathy^[5].
primary CD59 deficiency's subclass of is recorded as hereditary haemolytic anaemia due to red cell membrane defects^[6].
primary CD59 deficiency's MeSH descriptor ID is recorded as C567355^[7].
primary CD59 deficiency's OMIM ID is recorded as 612300^[8].
primary CD59 deficiency's Orphanet ID is recorded as 169464^[9].
primary CD59 deficiency's genetic association is recorded as CD59^[10].
primary CD59 deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_169464^[11].
primary CD59 deficiency's UMLS CUI is recorded as C2676767^[12].
primary CD59 deficiency's ICD-10-CM is recorded as D84.1^[13].
primary CD59 deficiency's Mondo ID is recorded as MONDO_0012858^[14].
primary CD59 deficiency's UniProt disease ID is recorded as DI-01329^[15].

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Quick Facts

Instance of rare disease, class of disease

Subclass of immunodeficiency due to a complement regulatory deficiency, genetic peripheral neuropathy, hereditary haemolytic anaemia due to red cell membrane defects

Properties

Exact match www.orpha.net

Genetic association CD59

Imported from wholeness_audit_2026-05-02

External References (7)

Icd-10-cm D84.1

Mesh descriptor id C567355

Mondo id MONDO_0012858

Omim id 612300

Orphanet id 169464

Umls cui C2676767

Uniprot disease id DI-01329

References

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

Direct Wikidata claims

[2] ↑ primary CD59 deficiency — instance of (P31): rare disease. wikidata.org.
[3] ↑ primary CD59 deficiency — instance of (P31): class of disease. wikidata.org.
[4] ↑ primary CD59 deficiency — subclass of (P279): immunodeficiency due to a complement regulatory deficiency. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[5] ↑ primary CD59 deficiency — subclass of (P279): genetic peripheral neuropathy. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[6] ↑ primary CD59 deficiency — subclass of (P279): hereditary haemolytic anaemia due to red cell membrane defects. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[7] ↑ primary CD59 deficiency — MeSH descriptor ID (P486): C567355. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[8] ↑ primary CD59 deficiency — OMIM ID (P492): 612300. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[9] ↑ primary CD59 deficiency — Orphanet ID (P1550): 169464. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[10] ↑ primary CD59 deficiency — genetic association (P2293): CD59. Paroxysmal nocturnal hemoglobinuria due to hereditary nucleotide deletion in the HRF20 (CD59) gene. Retrieved 2023-08-24. platform.opentargets.org. Provenance: wikidata.org.
[11] ↑ primary CD59 deficiency — exact match (P2888): http://www.orpha.net/ORDO/Orphanet_169464. wikidata.org.
[12] ↑ primary CD59 deficiency — UMLS CUI (P2892): C2676767. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[13] ↑ primary CD59 deficiency — ICD-10-CM (P4229): D84.1. Monarch Disease Ontology release 2018-06-29. Retrieved 2018-07-28. wikidata.org.
[14] ↑ primary CD59 deficiency — Mondo ID (P5270): MONDO_0012858. wikidata.org.
[15] ↑ primary CD59 deficiency — UniProt disease ID (P11430): DI-01329. wikidata.org.

Class ancestry

[1] ↑ primary CD59 deficiency is an instance of rare disease (Q929833) [P31, primary]. Wikidata. wikidata.org.

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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). primary CD59 deficiency. Retrieved May 3, 2026, from https://4ort.xyz/entity/primary-cd59-deficiency

MLA

“primary CD59 deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/primary-cd59-deficiency.

BibTeX

@misc{4ortxyz_primary-cd59-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{primary CD59 deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/primary-cd59-deficiency}, note = {Accessed: 2026-05-03}}

LLM prompt

According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): primary CD59 deficiency — https://4ort.xyz/entity/primary-cd59-deficiency (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/primary-cd59-deficiency · Last refreshed: May 3, 2026