Aliases: LGR3.
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 |
|---|---|---|
| Congenital Hypothyroidism | causative |
mechanism: Thyroid Gland Dysgenesis
subtype: TSHR Resistance
computational model: Minimal Hypothalamic-Pituitary-Thyroid Feedback Model
scoped to subtype: Permanent Primary
|
| Graves' Disease |
untyped
Risk Factor
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.