Genopathy
Gene-Disorder Association · Article
Gene
CD3D
CD3 Delta Subunit Of T-Cell Receptor Complex
Disorder
Hemolytic Uremic Syndrome, Atypical 6
First reported 2007
Key publication · disorder Hemolytic uremic syndrome (HUS) secondary to cobalamin C (cblC) disorder.Pediatric nephrology (Berlin, Germany) · 2007
Manually curated
Association Review

In brief

The association between CD3D (CD3 Delta Subunit Of T-Cell Receptor Complex) and Hemolytic Uremic Syndrome, Atypical 6 is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 21
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

Request access
03
CD3D

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

Request access
04
Hemolytic Uremic Syndrome, Atypical 6

The disorder

5 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Phenotype

Clinical features

12 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
06
Provenance

References & sources

4 references

Every source and publication cited across this dossier, as one numbered reference list.

Request access