NFE2L1

nuclear factor, erythroid 2 like 1
OMIM: 163260, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red NFE2L1 in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Syndromic disease, MONDO:0002254

Red NFE2L1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Syndromic disease, MONDO:0002254