ADGRL1

adhesion G protein-coupled receptor L1
OMIM: 616416, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber ADGRL1 in Early onset or syndromic epilepsy


Level 2: Neurology
Version 9.74
Latest signed off version: v9.56 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Developmental delay, behavioral abnormalities, and neuropsychiatric disorders, OMIM:620065
    Green ADGRL1 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.28
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Developmental delay, behavioral abnormalities, and neuropsychiatric disorders, OMIM:620065