FAAH2

fatty acid amide hydrolase 2
OMIM: 300654, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber FAAH2 in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.9
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Amber
    Tags
    • watchlist