ASMT

acetylserotonin O-methyltransferase
OMIM: 300015, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red ASMT in Mendeliome


Version 1.1891

review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services

Red ASMT in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review Unknown
Sources
  • Expert Review Red
  • Genetic Health Queensland