Hypothesis

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pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov

A homozygous variant in cardiac troponin I3, TNNI3, causes severe pediatric restrictive cardiomyopathy

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1. ClingenBaseline 07 Nov 2026
  
  in Baseline Annotations
  
  A homozygous variant in cardiac troponin I3, TNNI3, causes severe pediatric restrictive cardiomyopathy
  
  Gene:TNNI3 PMID:41918167 HGNC:11947 inferred_gene_hgnc:11947 inferred_gene_source:hgnc_tag Cardiomyopathy Annotation
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Tags

Gene:TNNI3

HGNC:11947

inferred_gene_hgnc:11947

Cardiomyopathy Annotation

inferred_gene_source:hgnc_tag

PMID:41918167

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ClingenBaseline

URL

pmc.ncbi.nlm.nih.gov/articles/PMC13096904/