Genopathy
Gene-Disorder Association · Article
Gene
KCNH2
Potassium Voltage-Gated Channel Subfamily H Member 2
Approved treatment annotated
Association Review

In brief

The association between KCNH2 (Potassium Voltage-Gated Channel Subfamily H Member 2) and Familial Hypertrophic Cardiomyopathy is supported by expert-curated evidence, drawing on a single expert-curated source, which records likely-pathogenic variants.

Sources 1
Clinical variants 1
Symptoms 0
Compounds 1
Trials 0of 329 via KCNH2 compounds
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
KCNH2

The gene

2 source summaries

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

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04
Familial Hypertrophic 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
ClinVar and variant evidence

Genetic basis

1 clinical variant

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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06
Interventions

Therapeutics

1 compound or drug

Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.

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07
Human studies

Clinical trials

329 clinical trials

Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.

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08
Provenance

References & sources

4 references

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

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