Genopathy
Gene-Disorder Association · Article
Gene
KCND3
Potassium Voltage-Gated Channel Subfamily D Member 3
Disorder
Long Qt Syndrome 11
First reported 1993
Key publication · disorder Long QT syndrome with insulin-dependent diabetes mellitus: contiguous gene syndrome on chromosome 11p.Journal of internal medicine · 1993
Manually curated
Association Review

In brief

The association between KCND3 (Potassium Voltage-Gated Channel Subfamily D Member 3) and Long Qt Syndrome 11 is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 3
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
KCND3

The gene

2 source summaries

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

Request access
04
Long Qt Syndrome 11

The disorder

9 database identifiers

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

Request access
05
Phenotype

Clinical features

2 clinical features

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

Request access
06
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

Request access
07
Provenance

References & sources

6 references

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

Request access