1. Genes and Genomic Entities
  2. LINGO1

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 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 Green
    • DD-Gene2Phenotype
    Phenotypes
    • LINGO1 related intellectual disability with microcephaly, speech and motor delay
    Amber LINGO1 in Intellectual disability

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 6.9
    Latest signed off version: v6.0 (1 May 2024)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • 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