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Rare familial disorder with hypertrophic cardiomyopathy
ORPHA:99739
Classification level: Group of disorders
- Rare familial disorder with hypertrophic obstructive cardiomyopathy
- Rare familial disorder with hypertrophic subaortic stenosis
Prevalence: -
Inheritance: Autosomal dominant
Age of onset:
UMLS: C5680311
MeSH: D024741
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
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Newborn screening