KLF13

KLF transcription 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 1.0

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 2.0

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 2.0

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