MEF2A

myocyte enhancer factor 2A
OMIM: 600660, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red MEF2A in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • {Coronary artery disease, autosomal dominant, 1} 608320