CCDC57

coiled-coil domain containing 57
ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red CCDC57 in Heterotaxy


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.45

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • Visceral heterotaxy, MONDO:0018677, CCDC57-related

Red CCDC57 in Mendeliome


Version 1.4556

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Visceral heterotaxy, MONDO:0018677, CCDC57-related

Red CCDC57 in Fetal anomalies


Version 1.543

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
  • Literature
Phenotypes
  • Visceral heterotaxy, MONDO:0018677, CCDC57-related