Previous symbols: ODG1. Aliases: FSHRO, LGR1.
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 |
|---|---|---|
| 46,XX Gonadal Dysgenesis | causative germline |
mechanism: FSHR Signaling Resistance
subtype: ODG1
scoped to subtype: ODG1
|
| Ovarian Hyperstimulation Syndrome | causative germline gain of function |
mechanism: Promiscuous FSH Receptor Activation by hCG or TSH
scoped to subtype: Familial Spontaneous OHSS
|
| Polycystic Ovary Syndrome |
untyped
Risk Factor
|
mechanism: Population-Specific Metabolic vs. Inflammatory Dysregulation
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.