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CD3delta deficiency

severe combined immunodeficiency that is characterized by the absence of T cells but normal numbers of B cells. CD3D is essential for T cell development
Class type of: severe combined immunodeficiency, T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta, autosomal recessive disease Q18965540

Facts

5 properties
Instance of
class of disease
Subclass of
severe combined immunodeficiency, T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta, autosomal recessive disease, primary immunodeficiency disease
Genetic association
CD3E[6]
Has phenotype
severe combined immunodeficiency[8]
On focus list of Wikimedia project
WikiProject Medicine[7]
🏷️ Also known as
en CD3D en CD3delta deficiency en Cd3-Epsilon Deficiency en IMD18 en IMMUNODEFICIENCY 18 en IMMUNODEFICIENCY 18; IMD18 en Immunodeficiency 18, SCID Variant en Immunodeficiency 18, Severe Combined Immunodeficiency Variant en Immunodeficiency type 18 fr déficit immunitaire combiné sévère T-B+ par déficit en CD3delta
🔖 Identifiers · 5
Disease Ontology ID
DOID:0060016
Exact match
purl.obolibrary.org, identifiers.org, www.orpha.net
Mondo ID
MONDO_0014278
OMIM ID
615615
UMLS CUI
C3810129, C3810128, C3810127

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Summary

CD3delta deficiency is a class of disease[1]. It is a type of severe combined immunodeficiency[2], T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta[3], autosomal recessive disease[4], and primary immunodeficiency disease[5].

References

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

Direct Wikidata claims

  1. [2] ↑ . Disease Ontology. Retrieved . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . Disease Ontology. Retrieved . wikidata.org.
  4. [5] ↑ . Disease Ontology. Retrieved . wikidata.org.
  5. [6] ↑ . UniProt. Retrieved . search.clinicalgenome.org. Provenance: wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . Disease Ontology. 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). CD3delta deficiency. Retrieved October 29, 2026, from https://4ort.xyz/entity/cd3delta-deficiency
MLA “CD3delta deficiency.” 4ort.xyz Knowledge Graph, 4ort.xyz, 29 Oct. 2026, https://4ort.xyz/entity/cd3delta-deficiency.
BibTeX @misc{4ortxyz_cd3delta-deficiency_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{CD3delta deficiency}}, year = {2026}, url = {https://4ort.xyz/entity/cd3delta-deficiency}, note = {Accessed: 2026-10-29}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): CD3delta deficiency — https://4ort.xyz/entity/cd3delta-deficiency (retrieved 2026-10-29)

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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. 18w ago · JhealdBatch bot · 2026-07-05 view diff on Wikidata ↗
    Mondo ID → MONDO_0014278
    UMLS CUI → C3810129, C3810128, C3810127
    Disease Ontology ID → DOID:0060016
    Genetic association → CD3E
    + 7 other properties edited (see Wikidata diff for full list)
    "Changed the item: QuickStatements 3.0 batch #39953: deprecate redundant disease superclasses (2)"
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