MAGED1

MAGE family member D1
OMIM: 300224, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red MAGED1 in Intellectual disability - microarray and sequencing

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 5.524
Latest signed off version: v5.0 (22 Mar 2023)

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 Red
    Phenotypes
    • X-linked syndrome characterized by intellectual disability