NDN

necdin, MAGE family member
OMIM: 602117, Gene2Phenotype

1 panel

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


Level 2: Developmental disorders
Version 9.285
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
    Sources
    • Literature
    Phenotypes
    • Smith-Magenis-like syndrome