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Amish nemaline myopathy and dilated cardiomyopathy caused by a homozygous contiguous gene deletion of TNNT1 and TNNI3 in a Mennonite child

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1. ClingenBaseline 09 Nov 2026
  
  in Baseline Annotations
  
  Amish nemaline myopathy and dilated cardiomyopathy caused by a homozygous contiguous gene deletion of TNNT1 and TNNI3 in a Mennonite child
  
  PMID: 30395933
  
  Gene: TNNT1
  
  HGNC ID: 11947
  
  OpenAccess Gene:TNNI1 HGNC:11947 inferred_gene_hgnc:11947 inferred_gene_source:hgnc_tag Cardiomyopathy Annotation
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inferred_gene_source:hgnc_tag

Cardiomyopathy Annotation

Gene:TNNI1

HGNC:11947

inferred_gene_hgnc:11947

OpenAccess

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ClingenBaseline

URL

pmc.ncbi.nlm.nih.gov/articles/PMC7237049/