Genopathy
Gene-Disorder Association · Article
Gene
ZFPM2
Zinc Finger Protein, FOG Family Member 2
Disorder
Conotruncal Heart Malformations
First reported 1950
Key publication · disorder Truncus arteriosus communis persistence.American heart journal · 1950
Manually curated
Association Review

In brief

The association between ZFPM2 (Zinc Finger Protein, FOG Family Member 2) and Conotruncal Heart Malformations is a manually-curated gene–disease association, drawing on a single expert-curated source, which records causative variation.

Sources 1
Clinical variants 0
Symptoms 9
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
ZFPM2

The gene

1 source summary

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

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04
Conotruncal Heart Malformations

The disorder

13 database identifiers

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

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05
Phenotype

Clinical features

9 clinical features

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

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06
Population genetics

GWAS signals

1 GWAS phenotype

Gene-associated GWAS phenotypes matching the disorder, with best SNP, score, risk-allele frequency and effect size.

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07
Provenance

References & sources

4 references

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

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