LHCGR Missense Mutation

Preferred Label : LHCGR Missense Mutation;

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

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

NCI Metathesaurus CUI : CL950748;

Details

Origin ID

C158721;

UMLS CUI

C5206924;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
molecular_abnormality_involves_gene
- LHCGR Gene [NCIt concept]

Keyword's position in hierarchy(ies) :

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