raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:217610

Neuromuscular 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
enNeuromuscular disease with dilated cardiomyopathy
frMaladie neuromusculaire avec cardiomyopathie dilatée
deNeuromuskuläre Krankheit mit dilatativer Kardiomyopathie
esEnfermedad neuromuscular con miocardiopatía dilatada
itMalattia neuromuscolare con cardiomiopatia dilatativa
nlNeuromusculaire ziekte met gedilateerde cardiomyopathie
ptDoença neuromuscular com miocardiopatia dilatada
plChoroba nerwowo-mięśniowa z kardiomiopatią rozstrzeniową
csNeuromuskulární choroba s dilatační kardiomyopatií
ukНервово-мязові захворювання з дилатаційною кардіоміопатією
zh神经肌肉疾病伴扩张型心肌病
trDilate kardiyomiyopatili nöromüsküler hastalık
2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
MONDO16334Evalidated
UMLSC5680878Evalidated

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 (10):

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