raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:324767

Non-familial rare disease with dilated 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
enNon-familial rare disease with dilated cardiomyopathy
frMaladie non familiale rare avec cardiomyopathie dilatée
deNicht-familiäre seltene Krankheit mit dilatativer Kardiomyopathie
esEnfermedad rara no familiar con miocardiopatía dilatada
itMalattia rara non familiare con cardiomiopatia dilatativa
nlNiet-familiale zeldzame ziekte met gedilateerde cardiomyopathie
ptDoença rara não familiar com miocardiopatia dilatada
plChoroba rzadka nierodzinna z kardiomiopatią rozstrzeniową
csNefamiliární vzácné onemocnění s dilatovanou kardiomyopatií
ukНесімейне рідкісне захворювання з дилатаційною кардіоміопатією
zh非家族性罕见病伴扩张型心肌病
trDilate kardiyomiyopati ile seyreden ailesel olmayan nadir hastalık
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO17952Evalidated
UMLSC5680960Evalidated

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