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hyper-IgM syndrome type 5

human disease
Class type of: hyper IgM syndrome, autosomal recessive disease Q5957527

Facts

5 properties
Instance of
rare disease, class of disease[4]
Subclass of
hyper IgM syndrome, autosomal recessive disease
Genetic association
UNG[5]
Has phenotype
childhood onset[7]
On focus list of Wikimedia project
WikiProject Medicine[6]
🏷️ Also known as
en IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5; HIGM5 en HIGM5 en hyper-IgM syndrome 5 en Hyper IgM syndrome 5 en hyper-IgM syndrome due to UNG deficiency en hyper-IgM syndrome due to uracil N-glycosylase en hyper-IgM syndrome type 5 en immunodeficiency with hyper IgM type 5 en IMMUNODEFICIENCY WITH HYPER-IgM, TYPE 5 de Hyper-IgM-Syndrom Typ 5 fr syndrome d'hyper-IgM type 5
🔖 Identifiers · 11
Disease Ontology ID
DOID:0060759
Exact match
purl.obolibrary.org, identifiers.org, www.orpha.net, www.orpha.net
Freebase ID
/m/0gv9cc
GARD rare disease ID
10581
ICD-10-CM
D80.5
Mondo ID
MONDO_0011971
OMIM ID
608106
Orphanet ID
183666, 101092
Raras disease ID
D101092
UMLS CUI
C1720958, C5190886
UniProt disease ID
DI-01812

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Summary

hyper-IgM syndrome type 5 is a rare disease[1]. It is a type of hyper IgM syndrome[2] and autosomal recessive disease[3].

References

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

Direct Wikidata claims

  1. [4] ↑ . wikidata.org.
  2. [2] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [3] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [5] ↑ . UniProt. Retrieved . platform.opentargets.org. Provenance: wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . Retrieved . 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 5. Retrieved November 7, 2026, from https://4ort.xyz/entity/hyper-igm-syndrome-type-5
MLA “hyper-IgM syndrome type 5.” 4ort.xyz Knowledge Graph, 4ort.xyz, 7 Nov. 2026, https://4ort.xyz/entity/hyper-igm-syndrome-type-5.
BibTeX @misc{4ortxyz_hyper-igm-syndrome-type-5_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hyper-IgM syndrome type 5}}, year = {2026}, url = {https://4ort.xyz/entity/hyper-igm-syndrome-type-5}, note = {Accessed: 2026-11-07}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hyper-IgM syndrome type 5 — https://4ort.xyz/entity/hyper-igm-syndrome-type-5 (retrieved 2026-11-07)

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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. 18d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    Has phenotype → childhood onset
    Raras disease ID → D101092
    Subclass of → hyper IgM syndrome, autosomal recessive disease
    "Changed labels, descriptions, aliases and claims: QuickStatements 3.0 batch #61469: Raras.org data import"
  2. 18w ago · JhealdBatch bot · 2026-07-04 view diff on Wikidata ↗
    Mondo ID → MONDO_0011971
    UMLS CUI → C1720958, C5190886
    Disease Ontology ID → DOID:0060759
    UniProt disease ID → DI-01812
    + 11 other properties edited (see Wikidata diff for full list)
    "Changed the item: QuickStatements 3.0 batch #39915: rm redundant disease superclass"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.