LHCGR Missense Mutation

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A point mutation in the LHCGR gene that encodes an amino acid substitution in the lutropin-choriogonadotropic hormone receptor protein.

**Synonyms:** - HHG Missense Mutation - LCGR Missense Mutation - LGR2 Missense Mutation - LH/CG-R Missense Mutation - LH/CGR Missense Mutation - LHCGR Missense Gene Mutation - LHR Missense Mutation - LHRHR Missense Mutation - LSH-R Missense Mutation - Luteinizing Hormone/Choriogonadotropin Receptor Missense Mutation - Non-synonymous LHCGR Gene Mutation - ULG5 Missense Mutation