FRYL

FRY like transcription coactivator
ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber FRYL in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 0.511

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Pan-Chung-Bellen syndrome, MIM# 621049

Amber FRYL in Mendeliome


Version 1.3795

3 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Pan-Chung-Bellen syndrome, MIM# 621049

Amber FRYL in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.507

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Pan-Chung-Bellen syndrome, MIM# 621049

Amber FRYL in Fetal anomalies


Version 1.482

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Pan-Chung-Bellen syndrome, MIM# 621049