ORPHA:83618

Severe dilated cardiomyopathy due to lamin A/C mutation

inactive · moved to ORPHA:300751Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Synonyms: Severe dilated cardiomyopathy with or without myopathy

Type: Disease
Group: Disorder
Status: inactive
Flag: Deprecated entity

This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Names in Orphadata languages

12 of 12 languages

Lang	Name	Synonyms
en	Severe dilated cardiomyopathy due to lamin A/C mutation	Severe dilated cardiomyopathy with or without myopathy
fr	Cardiomyopathie dilatée sévère due à une mutation du gène de la lamine A/C	Cardiomyopathie dilatée sévère avec ou sans myopathie
de	Kardiomyopathie, dilatative schwere, mit Lamin A/C-Mutationen	Kardiomyopathie, dilatative schwere, mit oder ohne Myopathie
es	Miocardiopatía dilatada grave por una mutación en el gen de la lamina A/C	Cardiomiopatía dilatada grave con o sin miopatía · Miocardiopatía dilatada grave con o sin miopatía
it	Cardiomiopatia dilatativa grave da mutazione di lamina A/C	Cardiomiopatia dilatativa grave con o senza miopatia
nl	Ernstige gedilateerde cardiomyopathie als gevolg van lamine A/C-mutatie	Ernstige gedilateerde cardiomyopathie met of zonder myopathie
pt	Cardiomiopatia dilatada grave por mutação na lamina A/C	Cardiomiopatia dilatada grave com ou sem miopatia
pl	Ciężka kardiomiopatia rozstrzeniowa z powodu mutacji laminy A/C	Ciężka kardiomiopatia rozstrzeniowa z miopatią lub bez miopatii
cs	Těžká dilatační kardiomyopatie způsobená mutací laminu A/C	Těžká dilatační kardiomyopatie s nebo bez myopatie
uk	Тяжка дилатаційна кардіоміопатія внаслідок мутації lamin A/C	Тяжка дилатаційна кардіоміопатія з міопією або без неї
zh	核纤层蛋白A/C基因突变所致严重扩张型心肌病症	严重扩张型心肌病伴或不伴肌病
tr	Lamin A / C mutasyonuna bağlı ağır dilate kardiyomiyopati	Miyopati ile seyreden veya seyretmeyen ağır dilate kardiyomiyopati

Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

Classification

Not placed in any Orphanet classification in this release.

No children.

Genes

0 direct

Orphanet records no gene directly on this code.

Prevalence and incidence

0 records

No prevalence record in this release.

HPO phenotypes

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

Sources for this card

Orphanet page: orpha.net/en/disease/detail/83618
This record as JSON: /data/d/83618.json