Variants
Sign InSign Up

Dilated cardiomyopathy 1AA

Your Results

Sign In

Description

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the ACTN2 gene.

MONDO

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

473

SEE THE VARIANTS →

Genes

External Links

  • OMIM

    612158

  • Orphanet
  • HPO
  • Medgen

    C2677338

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.