LINGO1

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

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Amber LINGO1 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Mental retardation, autosomal recessive 64, MIM# 618103

Amber LINGO1 in Microcephaly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.269

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Mental retardation, autosomal recessive 64, MIM# 618103

Amber LINGO1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Mental retardation, autosomal recessive 64, MIM#618103

Amber LINGO1 in Fetal anomalies


Version 1.255

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Mental retardation, autosomal recessive 64 - MIM#618103