Terminology Service for NFDI4Health
Familial Hypertrophic Cardiomyopathy Type 2
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http://purl.obolibrary.org/obo/NCIT_C142892
An autosomal dominant subtype of familial hypertrophic cardiomyopathy caused by mutation(s) in the TNNT2 gene, encoding troponin T, cardiac muscle. [ ]
Term info
Label
Familial Hypertrophic Cardiomyopathy Type 2
Synonyms
- CMH2
- Familial Hypertrophic Cardiomyopathy Type 2
NCI META CUI
CL541383
Preferred Name
Familial Hypertrophic Cardiomyopathy Type 2
Semantic Type
Disease or Syndrome
code
C142892