Terminology Service for NFDI4Health
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dilated cardiomyopathy 1A

Go to external page http://purl.obolibrary.org/obo/MONDO_0007269

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation is a rare familial dilated cardiomyopathy characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias including bradyarrhythmias, supraventricular or ventricular arrhythmias. Disease onset is usually in early to mid-adulthood. Sudden cardiac death may occur and may be the presenting symptom. In some cases, it is associated with skeletal myopathy and elevated serum creatine kinase. [ ]

Term info

Label

dilated cardiomyopathy 1A

Synonyms
  • CDCD1
  • LMNA familial isolated dilated cardiomyopathy
  • cardiomyopathy dilated with conduction defect type 1
  • cardiomyopathy, dilated, type 1A
  • dilated cardiomyopathy 1A
  • dilated cardiomyopathy type 1A
  • dilated cardiomyopathy with conduction defect 1
  • familial dilated cardiomyopathy with conduction defect due to LMNA mutation
  • familial isolated dilated cardiomyopathy caused by mutation in LMNA
database cross reference
Subsets

gard_rare, ordo_disease

exactMatch

http://purl.obolibrary.org/obo/Orphanet_300751, http://identifiers.org/snomedct/766883006, https://omim.org/entry/115200, http://purl.obolibrary.org/obo/DOID_0110425, http://linkedlifedata.com/resource/umls/id/C1449563

has related synonym

cardiomyopathy, idiopathic dilated, cardiomyopathy, dilated, 1A, cardiomyopathy, dilated, with conduction defect 1, cardiomyopathy, congestive, cardiomyopathy, familial idiopathic

id

MONDO:0007269

see also

https://rarediseases.info.nih.gov/diseases/1104/cardiomyopathy-dilated-with-conduction-defect-type-1