raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:217569

Rare hypertrophic cardiomyopathy

Type
Category
Group
Group of disorders
Status
active

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.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enRare hypertrophic cardiomyopathy
frCardiomyopathie hypertrophique rareMyocardiopathie hypertrophique rare
deSeltene hypertrophe Kardiomyopathie
esMiocardiopatía hipertrófica raraCardiomiopatía hipertrófica rara
itCardiomiopatia ipertrofica rara
nlZeldzame hypertrofische cardiomyopathie
ptMiocardiopatia hipertrófica rara
plRzadka kardiomiopatia przerostowaKardiomiopatia przerostowa zwężająca · Przerostowe zwężenie podaortalne
csVzácná hypertrofická kardiomyopatieHypertrofická subaortální stenóza · Hypertrofická obstrukční kardiomyopatie
ukРідкісна гіпертрофічна кардіоміопатія
zh肥厚型心肌病
trHipertrofik kardiyomiyopati
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO5045Evalidated
MeSHD002312Evalidated
UMLSC5680884Evalidated
MedDRA10020871Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (2):

Children (2):

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card