KLHL21

kelch like family member 21
OMIM: 616262, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red KLHL21 in Intellectual disability - microarray and sequencing

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.523
Latest signed off version: v5.0 (22 Mar 2023)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review Not set
    Sources
    • Expert Review Red