EIF3K

eukaryotic translation initiation factor 3 subunit K
OMIM: 609596, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber EIF3K in Mendeliome


Version 1.2667

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • EIF3K-related neurodevelopmental disorder, MONDO:0700092

Amber EIF3K in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 1.176

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Other
Phenotypes
  • EIF3K-related neurodevelopmental disorder, MONDO:0700092