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CD3gamma deficiency

Human disease
Class type of: severe combined immunodeficiency, non-severe combined immunodeficiency, autosomal recessive disease Q18553596

Facts

7 properties
Instance of
rare disease, class of disease[6]
Subclass of
severe combined immunodeficiency, non-severe combined immunodeficiency, autosomal recessive disease, T cell deficiency
Age of onset
infantile onset[8]
Genetic association
CD3G[7]
Has phenotype
Recurrent otitis media, chronic diarrhea, Recurrent respiratory infections, Recurrent oral thrush, failure to thrive, autoimmune hemolytic anemia, intestinal disease[10][11][12][13][14][15][16]
On focus list of Wikimedia project
WikiProject Medicine[9]
P14914
D169082[17]
🏷️ Also known as
en CD3 deficiency en Cd3-Gamma Deficiency en CD3gamma deficiency en IMD17 en IMMUNODEFICIENCY 17 en IMMUNODEFICIENCY 17; IMD17 en Immunodeficiency type 17 en SCID-Like Immunodeficiency, T Cell-Partial, B Cell-Positive, Nk Cell-Positive fr déficit immunitaire combiné par déficit en CD3gamma
🔖 Identifiers · 9
Disease Ontology ID
DOID:0060018, DOID:0111973
Exact match
purl.obolibrary.org, identifiers.org, www.orpha.net, purl.obolibrary.org, identifiers.org
GARD rare disease ID
9521
ICD-10-CM
D81.2
Mondo ID
MONDO_0014276
OMIM ID
615607
Orphanet ID
169082
UMLS CUI
C2025557, C3810107
UniProt disease ID
DI-04033

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Summary

CD3gamma deficiency is a rare disease[1]. It is a type of severe combined immunodeficiency[2], non-severe combined immunodeficiency[3], autosomal recessive disease[4], and T cell deficiency[5].

References

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

Direct Wikidata claims

  1. [6] ↑ . wikidata.org.
  2. [2] ↑ . Disease Ontology. Retrieved . wikidata.org.
  3. [3] ↑ . Monarch Disease Ontology release 2018-06-29. Retrieved . wikidata.org.
  4. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  6. [7] ↑ . UniProt. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  7. [8] ↑ . Retrieved . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . Retrieved . wikidata.org.
  10. [11] ↑ . Retrieved . wikidata.org.
  11. [12] ↑ . Retrieved . wikidata.org.
  12. [13] ↑ . Retrieved . wikidata.org.
  13. [14] ↑ . Retrieved . wikidata.org.
  14. [15] ↑ . Retrieved . wikidata.org.
  15. [16] ↑ . Retrieved . wikidata.org.
  16. [17] ↑ . 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). CD3gamma deficiency. Retrieved October 23, 2026, from https://4ort.xyz/entity/cd3gamma-deficiency
MLA “CD3gamma deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 23 Oct. 2026, https://4ort.xyz/entity/cd3gamma-deficiency.
BibTeX @misc{4ortxyz_cd3gamma-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{CD3gamma deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/cd3gamma-deficiency}, note = {Accessed: 2026-10-23}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): CD3gamma deficiency — https://4ort.xyz/entity/cd3gamma-deficiency (retrieved 2026-10-23)

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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. 16d ago · ACorrêa (WMB) · 2026-10-23 view diff on Wikidata ↗
    UniProt disease ID → DI-04033
    Mondo ID → MONDO_0014276
    Instance of → rare disease, class of disease
    GARD rare disease ID → 9521
    + 13 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||pt, pt-br */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/61469|batch #61469]]: Raras.org data import"
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