AMTN

amelotin
OMIM: 610912, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red AMTN in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert Review
Phenotypes
  • Amelogenesis imperfecta, type IIIB

Red AMTN in Amelogenesis imperfecta


Level 2: Skeletal disorders
Version 1.10

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Genomics England PanelApp
Phenotypes
  • Amelogenesis imperfecta, type IIIB