GRHL3

grainyhead like transcription factor 3
OMIM: 608317, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green GRHL3 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Van der Woude syndrome 2 MIM#606713

Green GRHL3 in Clefting disorders

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.252

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Van der Woude syndrome 2 MIM#606713

Green GRHL3 in Fetal anomalies


Version 1.255

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Genomics England PanelApp
Phenotypes
  • Van der Woude syndrome 2 MIM#606713