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hyper-IgM syndrome type 2

human disease
MedicalCondition rare_disease Q5957516
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hyper-IgM syndrome type 2

Summary

hyper-IgM syndrome type 2 is a rare disease[1].

Key Facts

  • hyper-IgM syndrome type 2's instance of is recorded as rare disease[2].
  • hyper-IgM syndrome type 2's instance of is recorded as class of disease[3].
  • hyper-IgM syndrome type 2 is a type of hyper IgM syndrome[4].
  • hyper-IgM syndrome type 2 is a type of hyperimmunoglobulin syndrome[5].
  • hyper-IgM syndrome type 2 is a type of genetic disease[6].
  • hyper-IgM syndrome type 2 is a type of autosomal recessive disease[7].
  • hyper-IgM syndrome type 2's NCI Thesaurus ID is recorded as C129074[8].
  • hyper-IgM syndrome type 2's genetic association is recorded as AICDA[9].
  • hyper-IgM syndrome type 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060758[10].
  • hyper-IgM syndrome type 2's exact match is recorded as http://identifiers.org/doid/DOID:0060758[11].
  • hyper-IgM syndrome type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101089[12].
  • hyper-IgM syndrome type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_183666[13].
  • hyper-IgM syndrome type 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [6] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [7] ↑ . Disease Ontology. Retrieved . wikidata.org.
  7. [8] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  8. [9] ↑ . Q905695. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  9. [10] ↑ . Disease Ontology. Retrieved . wikidata.org.
  10. [11] ↑ . Identifiers.org. registry.identifiers.org. Provenance: wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. 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). hyper-IgM syndrome type 2. Retrieved May 3, 2026, from https://4ort.xyz/entity/hyper-igm-syndrome-type-2
MLA “hyper-IgM syndrome type 2.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hyper-igm-syndrome-type-2.
BibTeX @misc{4ortxyz_hyper-igm-syndrome-type-2_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hyper-IgM syndrome type 2}}, year = {2026}, url = {https://4ort.xyz/entity/hyper-igm-syndrome-type-2}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hyper-IgM syndrome type 2 — https://4ort.xyz/entity/hyper-igm-syndrome-type-2 (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 · 2026-07-04 view diff on Wikidata ↗
    Nci thesaurus id → C129074
    On focus list of wikimedia project → WikiProject Medicine
    Gard rare disease id → 10578
    Imported from → —
    + 14 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/39915|batch #39915]]: rm redundant disease superclass"
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