Previous symbols: HHG. Aliases: LHR, LCGR, LGR2, ULG5.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Familial Male-limited Precocious Puberty | causative germline gain of function |
mechanism: Constitutive LHCGR Activation
|
| Polycystic Ovary Syndrome |
untyped
Risk Factor
|
mechanism: Population-Specific Metabolic vs. Inflammatory Dysregulation
|
| Ovarian Hyperstimulation Syndrome | no genetic record |
mechanism: hCG-Driven Luteinization of the Recruited Cohort
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.