Skip to content
New issue

Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.

By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.

Already on GitHub? Sign in to your account

Review classificiation of arrhythmogenic cardiomyopathy genetic subtypes (and Naxos disease) #1304

Open
allenbaron opened this issue Feb 21, 2024 · 1 comment
Assignees

Comments

@allenbaron
Copy link
Collaborator

Arrhythmogenic cardiomyopathy now consists of 3 major subtypes: right ventricular, biventricular, and left ventricular. Previously, they were all considered right ventricular. OMIM & DO still have them named this way and grouped together (in DO they're all children of 'arrhythmogenic right ventricular cardiomyopathy' (DOID:0050431).

We need to review the genetic subtypes to determine which are right, left, or biventricular. The left ventricular and biventricular subtypes were added in response to #1280. Orphanet xrefs also need to be revised & added.

We should also consider adding a grouping parent for these 3 subtypes. The natural choice would be 'arrhythmogenic cardiomyopathy' but the term has also been proposed as a broader grouping for various heart diseases, which complicates matters. An alternative could be 'inherited arrhythmogenic cardiomyopathy'.

The broader term “Arrhythmogenic cardiomyopathy, ACM” is currently used to encompass the whole spectrum of the abovementioned disease phenotypic expressions [7]. This term should not be confused with the one of “arrhythmogenic cardiomyopathies”, which has been proposed to comprise a series of different conditions that share non-ischemic myocardial scarring and the propensity to scar-related VAs [7].
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8268983/

Supporting information can be found in Curation_Review-arrhythmogenic_cardiomyopathy google doc and the corresponding OMIM inventory sheet, which shows that DO has all the OMIM subtypes.

Consider reviewing the classification of 'Naxos disease'(DOID:0080551) as part of this work as well.

Potentially relevant publications:

@allenbaron
Copy link
Collaborator Author

allenbaron commented Feb 21, 2024

May also be useful:

Also may need to update associated genes listed in definitions (some are missing genes).

Sign up for free to join this conversation on GitHub. Already have an account? Sign in to comment
Labels
None yet
Projects
None yet
Development

No branches or pull requests

2 participants