1. Genes and Genomic Entities
  2. NDN

NDN

necdin, MAGE family member
OMIM: 602117, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red NDN in Genomic imprinting


Version 0.149

review MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Sources
  • Literature
Phenotypes
  • Smith-Magenis-like syndrome
  • Prader-Willi syndrome 176270
Red NDN in Intellectual disability

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 6.13
Latest signed off version: v6.0 (1 May 2024)

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