Familial-genetic hypertrophic cardiomyopathy (Q42312): Difference between revisions
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Cardiomiopatia hipertrófica isolada familiar é a presença de cardiomiopatia hipertrófica não sindrômica em vários membros de uma linhagem ou na presença de uma mutação genética conhecida por estar significativamente associada a cardiomiopatia hipertrófica. | |||
| description / en | description / en | ||
Familial isolated hypertrophic cardiomyopathy is the presence of non-syndromic hypertrophic cardiomyopathy in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with hypertrophic cardiomyopathy. | |||
Revision as of 08:45, 13 August 2026
Familial isolated hypertrophic cardiomyopathy is the presence of non-syndromic hypertrophic cardiomyopathy in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with hypertrophic cardiomyopathy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | BC43.10 |
||
| English | Familial-genetic hypertrophic cardiomyopathy |
Familial isolated hypertrophic cardiomyopathy is the presence of non-syndromic hypertrophic cardiomyopathy in multiple members of a pedigree, or in the presence of a genetic mutation known to be significantly associated with hypertrophic cardiomyopathy. |
