raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:217678

Unclassified 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
enUnclassified cardiomyopathy
frCardiomyopathie non classée
deKardiomyopathie, nicht klassifizierte
esMiocardiopatía no clasificadaCardiomiopatía no clasificada
itCardiomiopata non classificata
nlNiet-geclassificeerde cardiomyopathie
ptMiocardiopatia não-classificada
plKardiomiopatia niesklasyfikowana
csNeklasifikovaná kardiomyopatie
ukНекласифікована кардіоміопатія
zh未分类心肌病
trSınıflandırılmamış kardiyomiyopati
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO16343Evalidated
UMLSC4682345Evalidated

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 (1):

Children (5):

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