LINGO1

leucine rich repeat and Ig domain containing 1
OMIM: 609791, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green LINGO1 in DDG2P


Version 8.1
Latest signed off version: v8.0 (12 Aug 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • DD-Gene2Phenotype
    Phenotypes
    • LINGO1 related intellectual disability with microcephaly, speech and motor delay
    Amber LINGO1 in Intellectual disability


    Level 2: Developmental disorders
    Version 11.1
    Latest signed off version: v11.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Hypotonic infant
  • Leukodystrophy, childhood onset
  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Radboud University Medical Center, Nijmegen
    • Literature
    Phenotypes
    • Mental retardation, autosomal recessive 64 (MIM 618103)
    Tags
    • watchlist