hypertrophic cardiomyopathy 9
Findings
No curated finding names hypertrophic cardiomyopathy 9 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 TTN gene.
Definition from the Mondo Disease Ontology (MONDO:0013412), read 2026-09-29. CC BY 4.0.
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Adult onset
HPO, annotations 2026-09-02
Features
1 feature
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
- 1 of 1 reported patient
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.
- TTNHGNC:12403
- Limited · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2017
Where it sits
Other names
6 names
Resolves to: hypertrophic cardiomyopathy 9
- Also called
- cardiomyopathy, familial hypertrophic, 9cardiomyopathy, familial hypertrophic, type 9CMH9hypertrophic cardiomyopathy caused by mutation in TTNhypertrophic cardiomyopathy type 9TTN hypertrophic cardiomyopathy