LGR4

leucine rich repeat containing G protein-coupled receptor 4
OMIM: 606666, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Amber LGR4 in Mendeliome


Version 1.1891

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • {Bone mineral density, low, susceptibility to} MIM#615311
  • Delayed puberty, self-limited MIM#619613
  • Syndromic disease, LGR4-related (MONDO#0002254)