KLF13

Kruppel like factor 13
OMIM: 605328, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber KLF13 in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 0.484

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Congenital heart disease MONDO:0005453 - KLF13-related

Amber KLF13 in Dilated Cardiomyopathy


Level 2: Cardiovascular disorders
Version 1.53

Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel
  • 1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Dilated cardiomyopathy - MONDO:0005021, KLF13-related

    Amber KLF13 in Mendeliome


    Version 1.3664

    1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Congenital heart disease MONDO:0005453 - KLF13-related
    • Dilated cardiomyopathy - MONDO:0005021, KLF13-related