FRYL

FRY like transcription coactivator
ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green FRYL in Congenital Heart Defect


Level 2: Cardiovascular disorders
Version 0.430

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

Green FRYL in Mendeliome


Version 1.2302

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

Green FRYL in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.63

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

Green FRYL in Fetal anomalies


Version 1.313

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