hypertrophic cardiomyopathy 7
Findings
No curated finding names hypertrophic cardiomyopathy 7 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNI3 gene.
Definition from the Mondo Disease Ontology (MONDO:0013369), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Adult onset
HPO, annotations 2026-09-02
Features
3 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Hypertrophic cardiomyopathyHPOHP:0001639
- 2 of 2 reported patients
- Apical hypertrophic cardiomyopathyHPOHP:0031992
- 3 of 6 reported patients
- Wolff-Parkinson-White syndromeHPOHP:0001716
- 3 of 6 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- TNNI3HGNC:11947
- Definitive · G2P · Autosomal dominant · 2024
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2021
Where it sits
- A kind of
Other names
6 names
Resolves to: hypertrophic cardiomyopathy 7
- Also called
- cardiomyopathy, familial hypertrophic, type 7cardiomyopathy, hypertrophic, 7CMH7hypertrophic cardiomyopathy caused by mutation in TNNI3hypertrophic cardiomyopathy type 7TNNI3 hypertrophic cardiomyopathy