ELFN1

extracellular leucine rich repeat and fibronectin type III domain containing 1
OMIM: 614964, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red ELFN1 in DDG2P


Version 4.3
Latest signed off version: v4.0 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • ELFN1-related intellectual disability and epilepsy