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Rare hypertrophic cardiomyopathy

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ORPHA:217569

Classification level: Group of disorders

Prevalence: -

Inheritance: -

Age of onset:

UMLS: C5680884

MeSH: D002312

MedDRA: 10020871

Summary

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.

Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

General public
Article for general public
Deutsch (2015.pdf) - BVHK
Guidelines
Emergency guidelines
Français (2018.pdf) - Orphanet Urgences
Clinical practice guidelines
Français (2021) - PNDS Logo FSMR
Deutsch (2024) - AWMF
English (2020) - Circulation Logo ERN
Genetic testing
Guidance for genetic testing
English (2011) - Eur J Hum Genet
Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Newborn screening

The documents contained in this website are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.