Genopathy
Gene-Disorder Association · Article
Gene
TNNC1
Troponin C1, Slow Skeletal And Cardiac Type
Disorder
Arrhythmogenic Right Ventricular Cardiomyopathy
First reported 1981
Key publication · disorder Arrhythmogenic right ventricular dysplasia: a cause of ventricular tachycardia in children with apparently normal hearts.American heart journal · 1981
Manually curated
Association Review

In brief

The association between TNNC1 (Troponin C1, Slow Skeletal And Cardiac Type) and Arrhythmogenic Right Ventricular Cardiomyopathy is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
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.

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02
Provenance

Evidence and sources

1 source

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

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03
TNNC1

The gene

1 source summary

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

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04
Arrhythmogenic Right Ventricular Cardiomyopathy

The disorder

6 database identifiers

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

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05
Provenance

References & sources

2 references

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

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