NDN

necdin, MAGE family member
OMIM: 602117, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red NDN in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Prader-Willi syndrome, MIM# 176270

Red NDN in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review Unknown
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • Prader-Willi syndrome, MIM# 176270