autosomal dominant intellectual developmental disorder 38

Summary
Synonym
  • MRD38
  • PRELDS
  • autosomal dominant mental retardation 38
  • autosomal dominant non-syndromic intellectual disability 38
  • psychomotor retardation, epilepsy, and language disability syndrome
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the EEF1A2 gene on chromosome 20q13.33.
Super Class
autosomal dominant intellectual developmental disorder
Disease Ontology
DOID:0070068
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1917 EEF1A2 eukaryotic translation elongation factor 1 alpha 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
13628 Eef1a2 eukaryotic translation elongation factor 1 alpha 2
Displaying all 2 entries
Gene ID Gene Symbol Description Source
175975 eef-1A.1 Elongation factor 1-alpha
181044 eef-1A.2 Elongation factor 1-alpha

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024