Hypertrophic cardiomyopathy 9

Synonyms: Familial hypertrophic cardiomyopathy 9

Summary

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TTN gene. [from MONDO]

Available tests

77 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (77 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

TTN
295 tests
Also known as: CMD1G, CMH9, CMPD4, CMYP5, EOMFC, HMERF, LGMD2J, LGMDR10, MYLK5, SALMY, TMD, TTN
Summary: titin

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the cardiovascular system
- Hypertrophic cardiomyopathy
  Hypertrophic cardiomyopathy
  - MedGen UID: 2881
  - Concept ID: C0007194
  - Finding: Disease or Syndrome
  Abnormality of the cardiovascular system
  See: Feature record | Search on this feature

Reviews

Clinical resources

Practice guidelines

EuroGenetest, 2011
Clinical utility gene card for: hypertrophic cardiomyopathy (type 1-14).

Molecular resources

Consumer resources

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