EEF1D

eukaryotic translation elongation factor 1 delta
OMIM: 130592, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green EEF1D in Severe microcephaly


Level 2: Neurology
Version 9.3
Latest signed off version: v9.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • NHS GMS
  • Literature
Phenotypes
  • Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language, OMIM:621150
Green EEF1D in Intellectual disability


Level 2: Developmental disorders
Version 10.18
Latest signed off version: v10.0 (6 May 2026)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with thin corpus callosum, hypotonia, and absent language, OMIM:621150