TECR

trans-2,3-enoyl-CoA reductase
OMIM: 610057, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red TECR in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.11
Latest signed off version: v6.0 (1 May 2024)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review Not set
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Red
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • non-syndromic mental retardation
    Tags
    • founder-effect